Xunce Technology’s Revenue Surges 449% Half-on-Half: Is a Structural Revaluation to a Hundred-Billion Market Cap Camp on the Horizon? ACN Newswire

Xunce Technology’s Revenue Surges 449% Half-on-Half: Is a Structural Revaluation to a Hundred-Billion Market Cap Camp on the Horizon?

HONG KONG, Mar 27, 2026 - (ACN Newswire via SeaPRwire.com) - As AI accelerates into the inference era, enterprise-grade AI is achieving large-scale deployment, driving an exponential surge in Token consumption and ushering data demand into a new development stage. Against this backdrop, high-quality, structured and scenario-specific professional data has become critical for enterprises to forge core strategic competitiveness in the era of AI.As a leading provider of AI real-time data infrastructure and analysis services in China, Xunce Technology is rapidly solidifying its core position in AI data, driven by industry tailwinds, full-chain technological capabilities and diversified growth engines. Amid the unfolding landscape of the intelligent economy, this ten-year industry stalwart is entering a pivotal window for structural revaluation.Token Value Restructuring: Making Every Data Access Quantifiable and MonetizableFounded in 2016, Xunce Technology has built a full-chain technological system spanning data acquisition, cleansing, standardization, real-time computing and large- model optimization over a decade of development. With AI Data Agent at its core, the Company specializes in millisecond-level real-time data processing, serving a diversified portfolio of industries including finance, urban governance, high-end manufacturing, healthcare, robotics, satellite applications, low-altitude economy, electric power, power grids and energy.As the era of AI inference unfolds, Token is evolving from mere “fuel” to a form of “hard currency”. Maximizing the value of each individual Token has emerged as a central challenge in the large-model inference era. Today, general-purpose large models typically rely on a “computing power for precision” approach, where every inference run generates substantial wasteful Token consumption. Should inference fail, all Tokens expended in the process are lost entirely, which is a common pain-point plaguing general AI systems.By contrast, vertical AI solutions equip general large language models with an external industry “brain” powered by domain-specific data. At its core, such solutions optimize inference logic via business-aware models, enabling upfront task feasibility validation and eliminating Token waste at the source. With deep expertise in professional vertical domain data modeling, Xunce Technology leverages its extensive portfolio of high-quality, scenario-specific proprietary data to act as an “efficiency multiplier” for every Token invocation. This structure translates Token consumption into higher-precision outputs while securing maximal result certainty. Crucially, the Company is developing full-chain capabilities spanning data metering, pricing and settlement, enabling quantifiable and monetizable measurement for every data access. By elevating per-unit Token efficiency, it delivers enhanced business value to enterprise clients.Aligned with this strategy, Xunce’s platform features a “LEGO-inspired” modular architecture, enabling clients to flexibly compose modules tailored to their specific needs. This “assemble-on-demand, adapt-in-real-time” design fosters deep and long-term customer stickiness. The Company also employs a highly flexible pricing framework, with fees structured around module count, processing throughput and other key metrics. Supported by subscription, transaction-based and Token-based payment models, its pricing mechanism precisely aligns with diverse client demands.Currently, Xunce Technology is fully building a full-chain data measurement and settlement system. It is exploring pricing mechanisms tied to large model inference frequency and module usage count, allowing customers to pay for effective Tokens rather than raw computing power consumption.Inflection Point Reached, Profitability ConfirmedDriven by Token value restructuring and innovative business models, Xunce Technology has delivered robust performance and reached a historic inflection point. In H2 2025, the Company posted an adjusted net profit of RMB 50 million, achieving its first positive profitability. Meanwhile, revenue rose from RMB 197.85 million in H1 2025 to RMB 1,086.81 million in H2, representing a 449.32% quarter-on-quarter surge. Amid rapid business expansion, the Company has witnessed a substantial improvement in profitability.Explosive Revenue GrowthReturn to Profit in H2Doubled ARPU & Per Capita GrowthImproved Cash Flow & Operating Metrics+103% Y/YNarrowed by 33%+105% Y/YSignificant Improvement2025 full-year revenue YoY growth2025 full-year adjusted net loss2025 ARPU YoY growth2025 net operating cash flow+449% H/HRMB 50 million+135% Y/YAmple cash on hand in 20252025 H2 revenue HoH growth2025 H2 adjusted net profit2025 per capita revenue YoY growthAverage collection period decreased in 2025For the full year, the Company posted total operating revenue of RMB 1,284.66 million, representing a substantial year-on-year increase of 103.28% and successfully breaking the key milestone of RMB 1 billion in revenue. This signifies that the Company has evolved from an early-stage, technology-driven startup into a new era of platform-based development with scalable and replicable business models.Furthermore, the Company’s combined gross proceeds for 2025 amounted to approximately RMB 792.08 million, representing a substantial increase of 63.44% compared to approximately RMB 484.63 million in the previous year. In terms of adjusted net loss, after deducting one-off non-recurring gains and losses, the Company’s adjusted net loss for 2025 was RMB 54.84 million, representing a significant narrowing of 33% from RMB 82.37 million in 2024.Notably, the Company achieved combined gross margin of 62% in 2025, exceeding that of Cambricon (55%), a leading AI chip provider, and far outpacing general large- model developer Minimax (25.4%). This underscores its high-value strategic positioning and resilient business model in the AI data infrastructure sector.In terms of R&D investment, Xunce Technology has also maintained efficient growth conversion. In 2025, the Company’s R&D expenditure reached RMB 450.44 million, with R&D expenses accounting for 48% of revenue, driving a 105% year-on-year increase in operating revenue. For comparison, Minimax’s R&D expenditure accounted for as high as 219% of its revenue, with a revenue growth rate of 159%. Xunce achieved a comparable expansion pace with a lower R&D intensity.As revenue scale continues to expand and gross margin in new industries gradually stabilize, the Company’s short-term objective is to achieve an inflection point in adjusted net profit. Looking ahead, as the industries already deployed enter a period of margin stabilization and Token-based payment and revenue-sharing models gain accelerated traction, its net profit is poised to improve at an accelerated rate.Driven by Diversified Growth Engines, Business Structure Continuously OptimizedThe robust revenue growth is not accidental, but underpinned by Xunce Technology’s multi-dimensional, systematically structured growth framework.Accelerate cross-industry replication. The Company currently covers 9 major industries, benchmarking Palantir’s 17 industries and leaving ample room for horizontal expansion. Xunce Technology is rapidly deepening its presence in key national strategic sectors such as asset management, telecommunications, electric power, urban management, high-end manufacturing, healthcare, energy, robotics training platforms and commercial aerospace. For each new industry, the Company first completes industry-specific data accumulation over 3 to 5 years, enabling rapid replication and scaled deployment across peer customers thereafter.The business model fosters deep customer value enhancement. As customers evolve from single-module adoption to multi-module deployment, and from pilot trials to full integration into core business workflows, substantial upside potential in ARPU remains. By synergistically lifting Token invocation volume, module usage count and per-Token value, the Company will unlock a new dimension of growth.Steadily expand overseas business and establish a global layout. The Company targets raising its overseas revenue share to 10% to 15% in 2026, and will further escalate its globalization strategy during 2027 and 2028, unlocking new avenues for sustained long-term growth.Cultivate a strategic cooperative ecosystem to forge deep integration with upstream and downstream partners in computing power and algorithms. Xunce Technology is engaging in in-depth collaboration with leading domestic GPU providers and large language model enterprises to build a one-stop solution encompassing “infrastructure computing power, upper-layer applications and data governance,” further solidifying its core position in the AI data infrastructure sector. Pioneer cutting-edge applications to seize commanding heights in future industries. From robotics data platforms to commercial aerospace, low-altitude economy and power grid systems, Xunce Technology has taken the lead in extending AI infrastructure to emerging sectors with stringent demands for real-time performance and operational reliability. Such mission-critical scenarios with ultra-high requirements for data timeliness and stability serve as a rigorous validation of the Company’s technological advantages. The Company will continue to ramp up R&D investment in frontier fields, refine its technical capabilities through high-end application scenarios and unlock new high-growth, high-value growth tracks for long-term development.Evolving from Data Services to Core AI Economy Infrastructure: Building Sustainable Competitive BarriersFrom a macro perspective, the artificial intelligence data sector is witnessing a profound convergence of five defining trends: a surge in demand for real-time, secure, high-quality data in the era of AI Agent; the rise of domain-specific models elevating professional data as a critical enabler for industry-wide intelligent upgrading; standardization of data interfaces driven by next-generation AI operating systems including Open Claw, positioning Xunce Technology as a core data Token provider; Token-based payment emerging as a new paradigm for the data element market; and the implementation of data asset capitalization policies, spurring a sharp rise in enterprises’ mandatory investment in data governance.At the intersection of these five pivotal trends, Xunce Technology has established a robust fundamental logic for sustained long-term growth. The Company has evolved beyond a traditional data infrastructure provider to become a critical “connector” and “enabler” linking large models, computing power and cloud vendors. By integrating upstream models, downstream computing power and horizontal collaboration with cloud vendors, the Company delivers irreplaceable data-centric value to its enterprise clients.The Company stresses that it shares a natural upstream-downstream synergy with general large-model providers, rather than a competitive dynamic. Analogous to the deep collaboration between GPU manufacturers and model developers, the value of Xunce Technology lies in a mutually reinforcing cycle: the wider the adoption of models by its clients, the greater the opportunity for the Company to deliver services and generate incremental value for clients.Notably, in contrast to niche market players offering only isolated modules such as data cleansing or computing engines, Xunce Technology’s core differentiation lies in its full-process coverage and outcome-driven accountability. The Company provides an end-to-end solution spanning data acquisition, cleansing, standardization, modeling, real-time computing and model tuning, ensuring that final data delivered to clients is clean, accurate, real-time and accessible for model invocation at millisecond latency. Furthermore, through deep integration into clients’ private clouds or on-premises environments, the Company acts as a dedicated data steward, fostering exceptional customer stickiness and forging robust, sustainable competitive barriers.Currently, the Company’s product portfolio and solutions feature more than 300 functional modules, covering a full spectrum of scenarios from data infrastructure to upper-layer analytics applications. In 2025, its active paid clients base reached 230, with an outstanding customer retention rate of 90%. ARPU increased substantially from RMB 2.72 million in 2024 to RMB 5.59 million in 2025, representing a year-on-year growth of over 103%.As algorithms become increasingly open-source and computing power tends toward standardization, what truly sets companies apart lies in data — particularly industry data that has undergone sophisticated governance and can effectively empower large models. Backed by a decade of deep industry expertise, Xunce Technology has established a substantial and sustainable competitive barrier in this domain.ConclusionFrom an early-stage private equity tool provider to a cross-industry AI data infrastructure builder, and from a module supplier to a Token-priced core platform, Xunce Technology has remained committed to unlocking data as a scarce, strategic resource that is freely circulable, readily callable and empowered to drive high-quality decision-making.Amid the rapid emergence of new intelligent economic paradigms, the Company stands at the threshold of a fundamental structural revaluation, with the potential to enter the RMB 100-billion market cap camp. It is a competitor to none, but an indispensable partner to all. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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Application Submitted for LENVIMA(R) (lenvatinib) in Japan Seeking Approval of Additional Dosage and Administration for Combination with WELIREG(R) (belzutifan) for Renal Cell Carcinoma that has Progressed After Chemotherapy JCN Newswire

Application Submitted for LENVIMA(R) (lenvatinib) in Japan Seeking Approval of Additional Dosage and Administration for Combination with WELIREG(R) (belzutifan) for Renal Cell Carcinoma that has Progressed After Chemotherapy

TOKYO, Mar 27, 2026 - (JCN Newswire via SeaPRwire.com) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, “Eisai”) and MSD K.K. (Headquarters: Tokyo, Representative Director: Prashant Nikam, “MSD”), a subsidiary of Merck & Co., Inc., Rahway, NJ, USA, announced today that an application for LENVIMA® (lenvatinib), an orally available multiple receptor tyrosine kinase inhibitor (TKI) discovered by Eisai, has been submitted in Japan for the additional dosage and administration in combination with WELIREG® (belzutifan), the first-in-class oral hypoxiainducible factor-2 alpha (HIF-2α) inhibitor from MSD, for the treatment of unresectable or metastatic renal cell carcinoma that has progressed after chemotherapy.This application is based on the results of the Phase 3 LITESPARK-011 trial evaluating the dual regimen of LENVIMA plus WELIREG for the treatment of patients with advanced renal cell carcinoma (RCC) whose disease progressed on or after treatment with anti-programmed death receptor-1 (PD-1)/ programmed death-ligand 1 (PD-L1) therapy. The data from this trial were presented at the 2026 American Society of Clinical Oncology (ASCO) Genitourinary (GU) Cancers Symposium in February 2026. At a pre-specified interim analysis with a median follow-up of 29.0 months (range, 19.3-49.2), the LENVIMA plus WELIREG combination therapy demonstrated a statistically significant and clinically meaningful improvement in progression-free survival (PFS), one of the primary endpoints, reducing the risk of disease progression or death by 30% (HR=0.70 [95% CI, 0.59-0.84]; p=0.00007) compared to cabozantinib. The safety profile of this combination was consistent with those reported for each agent administered as monotherapy, and no new safety signals were identified.In 2022, approximately 435,000 people worldwide were newly diagnosed with kidney cancer, and about 156,000 people died from the disease. 1 In Japan, it is estimated that roughly 21,000 people were newly diagnosed and about 7,000 died in 2022.2 RCC accounts for approximately 85% of kidney cancers3, and the five-year survival rates for patients with stage III and IV RCC have been reported as 63%–78% and 27%–28%4, respectively, indicating that the disease still has a high unmet medical needs.LENVIMA is approved in combination with KEYTRUDA ® (pembrolizumab) in Japan for the first-line treatment of unresectable or metastatic RCC. WELIREG is approved in Japan for the treatment of unresectable or metastatic RCC that has progressed following cancer chemotherapy. Additionally, supplemental New Drug Applications (sNDA) for the LENVIMA and WELIREG combination therapy for the treatment of adult patients with advanced RCC with a clear cell component following a PD-1 or PDL1 inhibitor has been accepted by the U.S. Food and Drug Administration (FDA), with a PDUFA (Prescription Drug User Fee Act) target action date set for October 4, 2026.Eisai and MSD have been collaborating through the provision of information on LENVIMA in Japan since October 2018, and will work together to expedite the maximization of contribution to patients with cancer.About LENVIMA (lenvatinib)LENVIMA, discovered and developed by Eisai, is an orally available multiple receptor tyrosine kinase inhibitor that inhibits the kinase activities of vascular endothelial growth factor (VEGF) receptors VEGFR1 (FLT1), VEGFR2 (KDR), and VEGFR3 (FLT4). LENVIMA inhibits other kinases that have been implicated in pathogenic angiogenesis, tumor growth, and cancer progression in addition to their normal cellular functions, including fibroblast growth factor (FGF) receptors FGFR1- 4, the platelet derived growth factor receptor alpha (PDGFRα), KIT, and RET. In syngeneic mouse tumor models, LENVIMA decreased tumor-associated macrophages, increased activated cytotoxic T cells, and demonstrated greater antitumor activity in combination with an anti-PD-1 monoclonal antibody compared to either treatment alone. LENVIMA has been approved for the indications below.Thyroid cancer- Indication as monotherapy(Approved mainly in Japan, the United States, Europe, China and Asia)Japan: Unresectable thyroid cancerThe United States: The treatment of patients with locally recurrent or metastatic, progressive, radioiodine-refractory differentiated thyroid cancer (DTC)Europe: The treatment of adult patients with progressive, locally advanced or metastatic, differentiated (papillary/follicular/Hürthle cell) thyroid carcinoma (DTC), refractory to radioactive iodine (RAI)Hepatocellular carcinoma- Indication as monotherapy(Approved mainly in Japan, the United States, Europe, China and Asia)Japan: Unresectable hepatocellular carcinomaThe United States: The first-line treatment of patients with unresectable hepatocellular carcinoma (HCC)Europe: The treatment of adult patients with advanced or unresectable hepatocellular carcinoma (HCC) who have received no prior systemic therapy- Indication in combination with KEYTRUDA (generic name: pembrolizumab) and transarterial chemoembolization (Approved in China)Thymic carcinoma- Indication as monotherapy (Approved in Japan)Japan: Unresectable thymic carcinomaRenal cell carcinoma (In Europe other than the United Kingdom, the agent was launched under the brand name Kisplyx®)- Indication in combination with everolimus(Approved mainly in the United States, Europe and Asia) The United States: The treatment of adult patients with advanced renal cell carcinoma (RCC) following one prior anti-angiogenic therapyEurope: The treatment of adult patients with advanced renal cell carcinoma following one prior vascular endothelial growth factor (VEGF) targeted therapy- Indication in combination with KEYTRUDA(Approved mainly in Japan, the United States, Europe and Asia)Japan: Radically unresectable or metastatic renal cell carcinomaThe United States: The first-line treatment of adult patients with advanced renal cell carcinomaEurope: The first-line treatment of adult patients with advanced renal cell carcinomaEndometrial carcinoma- Indication in combination with KEYTRUDA(Approved mainly in Japan, the United States, Europe and Asia)Japan: Unresectable, advanced or recurrent endometrial carcinoma that progressed after cancer chemotherapyThe United States: The treatment of patients with advanced endometrial carcinoma that is pMMR or not microsatellite instability-high (MSI-H), as determined by an FDA-approved test, who have disease progression following prior systemic therapy in any setting and are not candidates for curative surgery or radiationEurope: The treatment of adult patients with advanced or recurrent endometrial carcinoma (EC) who have disease progression on or following prior treatment with a platinum-containing therapy in any setting and are not candidates for curative surgery.About WELIREG (belzutifan)WELIREG, Merck & Co., Inc., Rahway, NJ, USA’s, known as MSD outside of the United States and Canada, first-in-class hypoxia-inducible factor 2 alpha (HIF-2α) inhibitor, is an orally administered small-molecule designed to reduce transcription and expression of HIF-2α target genes associated with cellular proliferation, angiogenesis and tumor growth. By inhibiting HIF-2α signaling, WELIREG aims to disrupt key pathways certain tumors may use to adapt to low-oxygen conditions, including those that help promote abnormal blood vessel formation and support tumor survival. WELIREG has demonstrated antitumor activity in certain von Hippel-Lindau (VHL) diseaseassociated tumors, renal cell carcinoma and in pheochromocytoma or paraganglioma. As part of a broader clinical program, Merck & Co., Inc., Rahway, NJ, USA continues to research WELIREG monotherapy and combination approaches for people with genitourinary, breast and gynecologic cancers across a range of treatment settings to further define where HIF-2α inhibition may provide clinical benefit and to better understand which patients are most likely to respond. WELIREG has been approved in Japan for the treatment of certain von Hippel–Lindau (VHL) disease–associated tumors, as well as for unresectable or metastatic renal cell carcinoma that has progressed after chemotherapy.LITESPARK-011 ResultsData from LITESPARK-011 (ClinicalTrials.gov, NCT04586231) were presented at the ASCO GU Symposium held in February 2026. LITESPARK-011 is a randomized, open-label Phase 3 trial (ClinicalTrials.gov, NCT04586231) evaluating WELIREG in combination with LENVIMA compared to cabozantinib for the treatment of patients with advanced clear cell RCC that has progressed on or after anti-PD-1/L1 therapy. The dual primary endpoints are progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1) as assessed by blinded independent central review (BICR), and overall survival (OS). Secondary endpoints include objective response rate (ORR) per RECIST v1.1 as assessed by BICR, duration of response (DOR) per RECIST v1.1 as assessed by BICR, and safety. The trial enrolled 747 patients who were randomized to receive WELIREG (120 mg orally once daily) plus LENVIMA (20 mg orally once daily) or cabozantinib (60 mg orally once daily).At a pre-specified second interim analysis with a median follow-up of 29.0 months (range, 19.3- 49.2), WELIREG plus LENVIMA demonstrated a statistically significant and clinically meaningful improvement in the primary endpoint of PFS, reducing the risk of disease progression or death by 30% (HR=0.70 [95% CI, 0.59-0.84]; p=0.00007) compared to cabozantinib. For WELIREG plus LENVIMA, the median PFS was 14.8 months (95% CI, 11.2-16.6) versus 10.7 months (95% CI, 9.2-11.1) for cabozantinib. A trend toward improvement in overall survival (OS), the trial’s other primary endpoint, was also observed for WELIREG plus LENVIMA (HR=0.85 [95% CI, 0.68-1.05]; p=0.06075). The median OS was 34.9 months (95% CI, 27.5-NR) for WELIREG plus LENVIMA versus 27.6 months (95% CI, 24.0-31.4) for cabozantinib. The trial is continuing, and OS will be evaluated at a subsequent analysis per the clinical trial protocol. Regarding secondary endpoints, at the first interim analysis with a median follow-up of 19.6 months (range, 9.9-39.8), WELIREG plus LENVIMA met ORR, demonstrating a statistically significant improvement compared to cabozantinib. A confirmed ORR of 52.6% (95% CI, 47.3-57.7) was observed for WELIREG plus LENVIMA versus 39.6% (95% CI, 34.6-44.8) for cabozantinib. At the second interim analysis with a median follow-up of 29.0 months, the median DOR was 23.0 months (95% CI, 2.0-44.3+) for WELIREG plus LENVIMA versus 12.3 months (95% CI, 1.8+-35.9+) for cabozantinib. WELIREG plus LENVIMA was administered to 370 patients and cabozantinib was administered to 371 patients. Grade ≥3 treatment-related adverse events (TRAEs) occurred in 71.6% of patients receiving WELIREG plus LENVIMA versus 65.8% of patients receiving cabozantinib. Adverse events led to treatment discontinuation in 11.1% of patients receiving WELIREG plus LENVIMA and in 11.3% of patients receiving cabozantinib, respectively. Serious adverse events were observed in 51.6% of patients receiving WELIREG plus LENVIMA versus 43.9% of patients receiving cabozantinib, and AEs led to death in 5.4% of patients (two were treatment-related: thrombotic microangiopathy [n=1] and pneumonitis [n=1]) versus 3.2% (one was treatment-related: hemoptysis [n=1]) of patients, respectively.About the Eisai and Merck & Co., Inc., Rahway, NJ, USA Strategic CollaborationIn March 2018, Eisai and Merck & Co., Inc., Rahway, NJ, USA through an affiliate, entered into a strategic collaboration for the worldwide co-development and co-commercialization of LENVIMA. Under the agreement, the companies jointly develop, manufacture and commercialize LENVIMA, both as monotherapy and in combination with Merck & Co., Inc., Rahway, NJ, USA’s anti-PD-1 therapy, KEYTRUDA, and HIF-2α inhibitor, WELIREG.Eisai’s focus on cancerEisai acknowledges “Oncology” as one of its key strategic areas, and will continue to focus on the discovery and development of anti-cancer drugs within drug discovery domains including “microenvironment”, “protein integrity and homeostasis”, and “cell lineage and cell differentiation” under the Deep Human Biology Learning (DHBL) drug discovery and development organization. Eisai aspires to discover innovative new drugs with new targets and mechanisms of action from these domains, with the aim of contributing to the cure of cancers.6. About EisaiEisai’s Corporate Concept is “to give first thought to patients and people in the daily living domain, and to increase the benefits that health care provides.” Under this Concept [also known as our human health care (hhc) Concept], we aim to effectively achieve social good in the form of relieving anxiety over health and reducing health disparities. With a global network of R&D facilities, manufacturing sites and marketing subsidiaries, we strive to create and deliver innovative products to target diseases with high unmet medical needs, with a particular focus in our strategic areas of Neurology and Oncology.In addition, our continued commitment to the elimination of neglected tropical diseases (NTDs), which is a target (3.3) of the United Nations Sustainable Development Goals (SDGs), is demonstrated by our work on various activities together with global partners. For more information about Eisai, please visit www.eisai.com (for global headquarters: Eisai Co., Ltd.), us.eisai.com (for U.S. headquarters: Eisai Inc.) or www.eisai.eu (for Europe, Middle East, Africa, Russia, Australia, and New Zealand headquarters: Eisai Europe Ltd.), and connect with us on X (U.S. and global), LinkedIn (for U.S. and EMEA) and Facebook (global).Merck & Co., Inc., Rahway, NJ, USA’s Focus on CancerEvery day, we follow the science as we work to discover innovations that can help patients, no matter what stage of cancer they have. As a leading oncology company, we are pursuing research where scientific opportunity and medical need converge, underpinned by our diverse pipeline of more than 25 novel mechanisms. With one of the largest clinical development programs across more than 30 tumor types, we strive to advance breakthrough science that will shape the future of oncology. By addressing barriers to clinical trial participation, screening and treatment, we work with urgency to reduce disparities and help ensure patients have access to high-quality cancer care. Our unwavering commitment is what will bring us closer to our goal of bringing life to more patients with cancer. For more information, visit https://www.merck.com/research/oncologyAbout MSDAt MSD (the name by which Merck & Co., Inc., Rahway, NJ, USA, is known outside of the United States and Canada), we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.co.jp and connect with us on Facebook, Twitter, and YouTube.Ferlay J, Ervik M, Lam F, Laversanne M, Colombet M, Mery L, et al. (2024) Global Cancer Observatory: Cancer Today. Lyon, France: International Agency for Research on Cancer. Available from: https://gco.iarc.who.int/media/globocan/factsheets/cancers/29-kidney-fact-sheet.pdf, accessed 27 Mar 2026.Ferlay J, Ervik M, Lam F, Laversanne M, Colombet M, Mery L, et al. (2024) Global Cancer Observatory: Cancer Today. Lyon, France: International Agency for Research on Cancer, Available from: https://gco.iarc.who.int/media/globocan/factsheets/populations/392-japan-fact-sheet.pdf, accessed 27 Mar 2026.National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology: Kidney Cancer. 2025; 2026 Version 1. Rose TL and Kim WY. Renal cell carcinoma: a review. JAMA. 2024 Sep 24;332(12):1001– 10.Media InquiriesEisai Co., Ltd.Public Relations DepartmentTEL: +81 (0)3-3817-5120MSD K.K.Communications DivisionTatsuro MuraseTEL: +81 (0)70-8700-0112 Copyright 2026 JCN Newswire via SeaPRwire.com. All rights reserved. www.jcnnewswire.com
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Hitachi and MUFG Bank expand NextGen model to finance vehicles and charging infrastructure for decarbonized mobility JCN Newswire

Hitachi and MUFG Bank expand NextGen model to finance vehicles and charging infrastructure for decarbonized mobility

TOKYO, Mar 27, 2026 - (JCN Newswire via SeaPRwire.com) - Hitachi, Ltd. (TSE: 6501, “Hitachi”) and MUFG Bank, Ltd. (“MUFG Bank”), a consolidated subsidiary of Mitsubishi UFJ Financial Group, Inc. (TYO: 8306, “MUFG”) today announced a new Memorandum of Understanding (MoU) to expand NextGen, their business co-creation model. Building on their collaboration launched in May 2024*1 and further developed as announced in May 2025*2 , NextGen combines Hitachi’s technology and operational expertise with MUFG’s financial capabilities to accelerate the transition to decarbonized mobility.*1 MUFG’s Business Co-Creation and Investment into UK Battery as a Service project by Hitachi ZeroCarbon May 2024*2 Hitachi ZeroCarbon and MUFG unite technology expertise with financial support to accelerate fleet electrification May 2025NextGen was initially validated through a UK pilot project with First Bus, where the parties collaborated via a special purpose vehicle (SPV) to support the procurement and operation of electrification assets under a Battery-as-a-Service model. This expanded MoU extends NextGen beyond battery-focused structures, enabling broader and more scalable deployment across additional markets outside the UK and across a wider range of asset classes. These include emobility assets such as electric vehicles and charging infrastructure, associated energy management systems, and potentially extending to energy hubs supporting industrial assets, power grids and data centers.Hitachi and MUFG Bank will also develop and scale SPV structures to finance decarbonized mobility assets for fleet and transport operators. This approach removes capital constraints and accelerates implementation, enabling operators to focus on their core transport services. From Hitachi’s side, the initiative is led by its Strategic SIB Business Unit, bringing together expertise from across Hitachi including Hitachi Energy, as ‘One Hitachi’. Hitachi will also provide managed services for asset performance and lifecycle optimization, supported by data-driven solutions from Hitachi ZeroCarbon. Through this initiative, Hitachi aims to further advance and streamline mobility and charging infrastructure operations by expanding HMAX by Hitachi, a suite of next-generation solutions that embodies Lumada 3.0, differentiated by deep domain knowledge and AI.Electrifying commercial transport at pace will require an unprecedented deployment of vehicles, charging and energy infrastructure - alongside innovative financing models to support it. Global investment in electrified transport reached around US$750 billion in 2024, making it the largest segment of the energy transition worldwide*3 - yet many fleet operators face limited access to capital and the operational complexity of transitioning at scale. Against this backdrop, Hitachi and MUFG Bank aim to expand NextGen as a repeatable model to accelerate implementation by combining structured asset financing with managed services and data-driven optimization.*3 Sources: BloombergNEF’s Energy transition Investment Trends 2025In demonstration of the expanded pipeline, Hitachi ZeroCarbon and MUFG Bank have also entered into an MoU with Boreal Norge AS and its subsidiary Boreal Buss AS, one of Norway’s primary transport operators, providing transport services across several counties and employing around 3,000 employees across its fleet, which includes over 850 buses and 35 ferries. The parties will explore how they can support Boreal’s transition planning, de-risk operations, optimize services and strengthen competitiveness as concessions evolve.Jun Taniguchi, Senior Vice President and Executive Officer, CEO of Strategic SIB Business Unit, at Hitachi, Ltd. said:“We are delighted to advance this partnership which combines Hitachi’s deep expertise in social infrastructure and digital technologies with MUFG Bank, Ltd.’s financial strength to accelerate the transition to a decarbonized society. By improving the performance of assets such as batteries and charging infrastructure through Hitachi’s digital services led by HMAX, we can truly help customers optimize the total cost of ownership. This partnership embodies our One Hitachi approach, leveraging our diverse capabilities across the Group to support our customers in achieving their net-zero ambitions.”Masakazu Osawa, Senior Managing Executive Officer Chief Executive, Japanese Corporate & Investment Banking Business Unit of MUFG Bank, Ltd., said:“Building on MUFG’s Business Co‑Creation and Investment approach, this collaboration with Hitachi aims to create value through strategic partnerships that improve society and the environment. For the global EV market, our focus is not only on strengthening Hitachi’s leading position in Battery as a Service, but also on fostering a holistic value chain — including second‑ life battery markets — that supports the acceleration of electric mobility and the achievement of 2050 net‑zero targets. Together with our partners, we are committed to co‑creating sustainable businesses that become a driving force for progress worldwide.”Nikolai Knudsmoen Utheim, Group CEO, Boreal Norge AS said:“Our priority has always been to deliver first-class transport services to our customers, whether that’s on the road, rail or over water. In exploring how we can unlock the power of electrified fleets, we can not only deliver more sustainable operations, but upgrade our infrastructure and thread technology across our entire business model for more efficient, smart transport and energy management.”About Hitachi, Ltd.Through its Social Innovation Business (SIB) that brings together IT, OT (Operational Technology) and products, Hitachi contributes to a harmonized society where the environment, wellbeing, and economic growth are in balance. Hitachi operates globally in four sectors – Digital Systems & Services, Energy, Mobility, and Connective Industries – and the Strategic SIB Business Unit for new growth businesses. With Lumada at its core, Hitachi generates value from integrating data, technology and domain knowledge to solve customer and social challenges. Revenues for FY2024 (ended March 31, 2025) totaled 9,783.3 billion yen, with 618 consolidated subsidiaries and approximately 280,000 employees worldwide. Visit us at www.hitachi.com.About MUFGMitsubishi UFJ Financial Group, Inc. (MUFG) is one of the world’s leading financial groups. Headquartered in Tokyo and with over 360 years of history, MUFG has a global network with approximately 2,000 locations in more than 40 countries. The Group has about 150,000 employees and offers services including commercial banking, trust banking, securities, credit cards, consumer finance, asset management, and leasing. The Group aims to “be the world’s most trusted financial group” through close collaboration among our operating companies and flexibly respond to all of the financial needs of our customers, serving society, and fostering shared and sustainable growth for a better world. MUFG’s shares trade on the Tokyo, Nagoya, and New York stock exchanges. For more information, visit https://www.mufg.jp/english.About BorealBoreal is a leading mobility provider, operating buses, fast ferries, passenger ferries and trams in Norway and Sweden. We remain firmly committed to our societal mission of encouraging more people to travel collectively. At the same time, we are more than public transport. As the only company operating buses, ferries, fast ferries, trams and tourism services, we deliver integrated mobility solutions and travel experiences. Although Boreal is a young company in name, its heritage extends back more than 150 years. The company has around 3,000 employees and is headquartered in Stavanger, Norway. Copyright 2026 JCN Newswire via SeaPRwire.com. All rights reserved. www.jcnnewswire.com
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Analogue 2025 Annual Results Profit Attributable to Owners of the Company Increases 23.5% to HK$167.0 Million ACN Newswire

Analogue 2025 Annual Results Profit Attributable to Owners of the Company Increases 23.5% to HK$167.0 Million

HONG KONG, Mar 27, 2026 - (ACN Newswire via SeaPRwire.com) - Analogue Holdings Limited (“Analogue” or the “Company”, together with its subsidiaries, the “Group”) (stock code: 1977), a leading provider of electrical and mechanical (“E&M”) engineering solutions, and information and communications technology services for smart cities, today announced its annual results for the year ended 31 December 2025 (“the Year” or “FY2025”) with net profit growth, contracts-in-hand achieving another record high and order intake more than doubled, providing a solid business foundation for the coming three years and beyond.Financial Highlights- Profit attributable to owners of the Company increased 23.5% to HK$167.0 million.- Contracts-in-hand surged 61.8% to HK$17,878.7 million, hitting another record-high, made possible by a 113.7% increase in order intake to HK$12,913.6 million during the Year.- The intake of new maintenance contracts for housing programmes, environmental projects and lifts and escalators increased 51.4% to HK$1,669 million, reinforcing the recurring revenue stream.- The Group maintained a strong cash position, with bank balances and cash of HK$1,020.8 million and gearing ratio reduced to 10.1% for FY2025 from 26.2%.- The Board has resolved to pay a second interim dividend of HK2.9 cents per share. Total dividend for the year amounted to HK5.5 cents per share with 25.6% increment year-on-year.Chairman Dr Mak Kin Wah said, “The Year 2025 saw profound changes around the world, with challenges and yet also opportunities. Our Group has continued to stride forward: upholding what we commit by delivering the fundamentals well, striving for continuous improvement to make transformation actionable, investing in technology advancement and productivity, and bringing Hong Kong’s engineering excellence to the world. We are pleased to report that the Group achieved profit growth, secured a record level of contracts-in-hand, and continued to build on our international market presence. These accomplishments highlight our distinctive comprehensive capability across diverse business segments, our commitment to excellence, and our leadership in advanced engineering techniques.”“Supported by strong cashflow, we are in a strong position to take on additional work where appropriate and to seize high-value opportunities as they arise. We will continue to stay agile and focused on capturing opportunities across our broad portfolio, build on our competitive strengths through continuous improvement, and reinforce the use of innovative solutions that enhance quality, safety and performance. We remain steadfast in our commitment to our customers, recognising that this is fundamental to earning their trust and cultivating enduring, strategic partnerships. Guided by our motto – ‘We Commit. We Perform. We Deliver’ – we will continue to maximise value for customers, shareholders, suppliers and stakeholders, while contributing to the communities we serve.”Business Review: Building Services- This segment remains the largest revenue contributor, with revenue reaching HK$3,279 million.- Contracts-in-hand reached a record-high level of HK$8,297 million with the total value of new contracts secured in FY2025 doubled to HK$6,470 million. The Group’s competitive edge in multidisciplinary packaged projects and its industry leadership in innovative MiMEP and other new engineering techniques helped it to secure major contracts.- With strategic investments to accelerate innovation and modern manufacturing facilities in Zhuhai and Hong Kong, the Group continues to lead in MiMEP and DfMA technologies.- Following the successful acquisition of a property management licence, the Group expanded its business to deliver integrated solutions across the entire building lifecycle. This new capability, spanning construction, maintenance, operations and long-term facility management, creates a potential revenue stream that complements core services.- Through continuous development of innovative technologies and operational optimisation, the segment is positioning itself to maintain the market competitiveness while exploring opportunities in other markets in Southeast Asia.Environmental Engineering- This segment achieved record-high contracts-in-hand and order intake, increasing 86.9% and 253.7% to HK$8,094 million and HK$5,355 million respectively. Segment revenue also increased by 18.0% year-on-year to HK$1,591 million.- The segment maintained active tendering throughout the period and was awarded significant contracts, including contracts of a record-breaking value to relocate sewage treatment works in Sha Tin to caverns, sewage pumping station at Ma On Shan and more.- Formed a joint venture company in Qingyang city to explore the operation and maintenance business in the Chinese Mainland.- Explored project opportunities in Asia and the Middle East and the expansion of its expert services into Europe.Information, Communications and Building Technologies (“ICBT”)- Segment revenue remained at HK$630 million. Contracts-in-hand totalled HK$852 million at the year end, and order intake was HK$523 million during the Year.- This segment continued to reinforce its leadership in green and intelligent building solutions under the DigiFusion brand, to enable the development of smarter, more sustainable urban environments.- Continued to leverage ATAL Tower as a platform for developing innovative technologies and broaden its technological capabilities through strategic collaborations with leading manufacturers in the Chinese Mainland and around the world, to strengthen its ability to deliver scalable, high-performance solutions across a wide range of sectors.Lifts and Escalators- Revenue and order intake increased 11.0% to HK$587 million and by 3.2% to HK$566 million respectively.- Transel Elevator & Electric Inc. (TEI), the associate company in the United States (US), secured a contract for the world-class vertical transportation system in the iconic 56-storey luxury hotel skyscraper on the border of Times Square in New York. TEI also further strengthened its market position by extending its footprint into the Southeastern part of US.- Actively built on its presence in the UK and broadened its network across other international markets, reinforcing its global ambitions in vertical transportation solutions.- Machine-Room-Less lift products continued to gain traction in key international markets- Streamlined the manufacturing processes of Nanjing factory, broadened its product portfolio and strengthened the overall product quality, aligning with the Group’s global vision and reaffirming its commitment to delivering reliable, high-performance vertical transportation solutions.For further details of the 2025 Annual Results, please refer to the announcement filed with The Stock Exchange of Hong Kong Limited.About Analogue Holdings LimitedEstablished in 1977, Analogue Holdings Limited is a leading provider of electrical and mechanical (“E&M”) engineering solutions and information and communications technology (“ICT”) services for smart cities, with headquarters in Hong Kong and operations in the Chinese Mainland, Macau, the United States, the United Kingdom, Germany, Singapore and Malaysia. Serving a wide spectrum of customers from public and private sectors, the Group provides multidisciplinary and comprehensive E&M engineering and technology services in four major segments, including Building Services, Environmental Engineering, Information, Communications and Building Technologies (“ICBT”) and Lifts & Escalators.The Group also manufactures and sells lifts and escalators internationally and has entered into an alliance with Transel Elevator & Electric Inc. (“TEI”), one of the largest independent lifts and escalators companies in New York, the United States. The Group’s associate partner, Nanjing Canatal Data-Centre Environmental Tech Co., Ltd. (603912.SS), specialises in manufacturing of precision air conditioners. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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Stella McCartney Menyatakan Industri Mode Harus Berubah Saat Menerima TIME Earth Award Informasi

Stella McCartney Menyatakan Industri Mode Harus Berubah Saat Menerima TIME Earth Award

(SeaPRwire) - Desainer fashion yang dikenal karena advokasinya terhadap bahan berkelanjutan menerima TIME Earth Award pada hari Kamis di London.Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Eisai and Nuvation Bio Announce Marketing Authorisation Application for Taletrectinib for the Treatment of Advanced ROS1-Positive Non-Small Cell Lung Cancer Validated by the European Medicines Agency JCN Newswire

Eisai and Nuvation Bio Announce Marketing Authorisation Application for Taletrectinib for the Treatment of Advanced ROS1-Positive Non-Small Cell Lung Cancer Validated by the European Medicines Agency

TOKYO and NEW YORK, NY., Mar 27, 2026 - (JCN Newswire via SeaPRwire.com) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, “Eisai”), a human-centered global leading research-based pharmaceutical company working in the neurology and oncology therapeutic areas, and Nuvation Bio Inc. (NYSE: NUVB, Corporate Headquarters: New York, NY, CEO: David Hung, M.D., “Nuvation Bio”), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, today announced that the European Medicines Agency (EMA) has validated the Marketing Authorisation Application (MAA) for taletrectinib for the treatment of advanced ROS1-positive (ROS1+) non-small cell lung cancer (NSCLC). The filing will follow a standard review timeline.Taletrectinib (marketed as IBTROZI® in the U.S. and Japan) is a highly selective, next-generation oral treatment for patients living with advanced ROS1+ NSCLC.1 In January 2026, Eisai and Nuvation Bio announced they had entered into an exclusive licensing and collaboration agreement in Europe and additional countries* outside the U.S., China and Japan to extend the global reach of taletrectinib. Following this filing to the EMA, additional filings are planned for the U.K., Canada and other regions included in Eisai’s licensed territories.Across Europe, nearly 400,000 people are diagnosed with lung cancer each year with NSCLC accounting for 80% of cases.2,3 It is estimated that approximately 2% of patients with NSCLC have ROS1+ disease.4,5“The validation of the MAA is a significant moment for patients in Europe with ROS1+ NSCLC,” said Terushige Iike, Chief Business Officer of Eisai Co., Ltd. “With its efficacy and safety profile, we believe taletrectinib has the potential to become a standard of care therapy for the thousands of patients living with this aggressive disease in Europe. We look forward to working closely with the EMA during the review process with the goal of making this treatment available to appropriate patients who urgently need targeted options.”The application is based on data from the two pivotal Phase 2 clinical studies, TRUST-I and TRUST-II, evaluating taletrectinib in patients globally.6,7 Results from a pooled analysis of the TRUST clinical program were published in the Journal of Clinical Oncology in April 20258, and Nuvation Bio anticipates near-term disclosure of updated data reflecting even longer patient follow-up, further building on the depth and durability of responses observed to date. Additionally, given the comprehensive nature of the taletrectinib clinical dataset and based on favorable feedback received at a pre-submission meeting with the CHMP Rapporteur and Co-Rapporteur, the accepted MAA will be considered to support full approval.“Having seen the meaningful impact taletrectinib has already made for patients with ROS1+ NSCLC in the U.S., China and Japan, we are thrilled to partner with Eisai and have an accepted MAA for review in Europe,” said David Hung, M.D., Founder, President and Chief Executive Officer of Nuvation Bio. “This accepted filing represents an important milestone in our global development strategy and brings us one step closer to delivering this highly selective, next-generation oral therapy to more patients who need it in Europe and around the world.”In June 2025, the U.S. Food and Drug Administration (FDA) granted full approval to taletrectinib for the treatment of locally advanced or metastatic ROS1+ NSCLC across lines of therapy, following a Priority Review and double Breakthrough Therapy designations. Taletrectinib is also approved for patients with advanced ROS1+ NSCLC in Japan, where it is marketed by Nippon Kayaku, and in China, where it is marketed by Innovent Biologics under the brand name DOVBLERON®.* Eisai’s licensed territories: Europe, the Middle East, North Africa, Russia, Turkey, Canada, Australia, New Zealand, Singapore, the Philippines, Indonesia, Thailand, Malaysia, Vietnam and IndiaAbout ROS1+ NSCLCEach year, more than one million people globally are diagnosed with non-small cell lung cancer (NSCLC), the most common form of lung cancer.9 It is estimated that approximately 2% of patients with NSCLC have ROS1+ disease.4,5 About 35% of patients newly diagnosed with metastatic ROS1+ NSCLC have tumors that have spread to their brain.10 The brain is also the most common site of disease progression, with about 50% of previously treated patients developing central nervous system (CNS) metastases.10,11About TaletrectinibTaletrectinib is an oral, potent, CNS-active, selective, next-generation ROS1 inhibitor therapy. On June 11, 2025, following Priority Review and Breakthrough Therapy designations for both TKI-naive and TKI-pretreated disease, the U.S. Food and Drug Administration (FDA) approved taletrectinib for the treatment of adult patients with locally advanced or metastatic ROS1+ NSCLC. Learn more about taletrectinib in the U.S. at IBTROZI.com. 1About the TRUST Clinical ProgramThe TRUST clinical program comprises three registrational studies evaluating the safety and efficacy of taletrectinib. TRUST-I (NCT04395677) and TRUST-II (NCT04919811) are Phase 2 single-arm studies evaluating taletrectinib for the treatment of adults with advanced ROS1+ NSCLC in China (N=173) and globally (N=189), respectively. The primary endpoint of both studies is confirmed objective response rate (cORR) as assessed by an independent review committee. TRUST-IV (NCT07154706) is a Phase 3 placebo-controlled study evaluating taletrectinib for the adjuvant treatment of adults with resected early-stage ROS1+ NSCLC. The study will enroll approximately 180 patients in the U.S., Canada, Europe, Japan and China. The primary endpoint is disease-free survival as determined by investigator, and the primary completion date is estimated to be in 2030. Nuvation Bio is also sponsoring TRUST-III (NCT06564324), a confirmatory randomized Phase 3 study evaluating taletrectinib versus crizotinib in 138 patients in China with advanced ROS1+ NSCLC who have not previously received ROS1 TKIs.6,7About Eisai Co., Ltd.Eisai's Corporate Concept is "to give first thought to patients and people in the daily living domain, and to increase the benefits that health care provides." Under this Concept (also known as human health care (hhc) Concept), we aim to effectively achieve social good in the form of relieving anxiety over health and reducing health disparities. With a global network of R&D facilities, manufacturing sites and marketing subsidiaries, we strive to create and deliver innovative products to target diseases with high unmet medical needs, with a particular focus in our strategic areas of Neurology and Oncology.In addition, we demonstrate our commitment to the elimination of neglected tropical diseases (NTDs), which is a target (3.3) of the United Nations Sustainable Development Goals (SDGs), by working on various activities together with global partners.For more information about Eisai, please visit www.eisai.com (for global headquarters: Eisai Co., Ltd.), and connect with us on X, LinkedIn and Facebook. The website and social media channels are intended for audiences outside of the UK and Europe.About Nuvation BioNuvation Bio is a global oncology company focused on tackling some of the toughest challenges in cancer treatment with the goal of developing therapies that create a profound, positive impact on patients’ lives. Our diverse pipeline includes taletrectinib (IBTROZI®), a next-generation ROS1 inhibitor; safusidenib, a brain-penetrant IDH1 inhibitor; and an innovative drug-drug conjugate (DDC) program.Nuvation Bio was founded in 2018 by biopharma industry veteran David Hung, M.D., who previously founded Medivation, Inc., which brought to patients one of the world’s leading prostate cancer medicines. Nuvation Bio has offices in New York, San Francisco, Boston, and Shanghai. For more information, visit www.nuvationbio.com or follow the company on LinkedIn and X (@nuvationbioinc).U.S. IndicationIBTROZI is indicated for the treatment of adult patients with locally advanced or metastatic ROS1+ nonsmall cell lung cancer (NSCLC).IMPORTANT SAFETY INFORMATION FOR IBTROZI® (taletrectinib)1WARNINGS AND PRECAUTIONSHepatotoxicity: Hepatotoxicity, including drug-induced liver injury and fatal adverse reactions, can occur. 88% of patients experienced increased AST, including 10% Grade 3/4. 85% of patients experienced increased ALT, including 13% Grade 3/4. Fatal liver events occurred in 0.6% of patients. Median time to first onset of AST or ALT elevation was 15 days (range: 3 days to 20.8 months).Increased AST or ALT each led to dose interruption in 7% of patients and dose reduction in 5% and 9% of patients, respectively. Permanent discontinuation was caused by increased AST, ALT, or bilirubin each in 0.3% and by hepatotoxicity in 0.6% of patients.Concurrent elevations in AST or ALT ≥3 times the ULN and total bilirubin ≥2 times the ULN, with normal alkaline phosphatase, occurred in 0.6% of patients.Interstitial Lung Disease (ILD)/Pneumonitis: Severe, life-threatening, or fatal ILD or pneumonitis can occur. ILD/pneumonitis occurred in 2.3% of patients, including 1.1% Grade 3/4. One fatal ILD case occurred at the 400 mg daily dose. Median time to first onset of ILD/pneumonitis was 3.8 months (range: 12 days to 11.8 months).ILD/pneumonitis led to dose interruption in 1.1% of patients, dose reduction in 0.6% of patients, and permanent discontinuation in 0.6% of patients.QTc Interval Prolongation: QTc interval prolongation can occur, which can increase the risk for ventricular tachyarrhythmias (e.g., torsades de pointes) or sudden death. IBTROZI prolongs the QTc interval in a concentration-dependent manner.In patients who received IBTROZI and underwent at least one post baseline ECG, QTcF increase of >60 msec compared to baseline and QTcF >500 msec occurred in 13% and 2.6% of patients, respectively. 3.4% of patients experienced Grade ≥3. Median time from first dose of IBTROZI to onset of ECG QT prolongation was 22 days (range: 1 day to 38.7 months). Dose interruption and dose reduction each occurred in 2.8% of patients.Significant QTc interval prolongation may occur when IBTROZI is taken with food, strong and moderate CYP3A inhibitors, and/or drugs with a known potential to prolong QTc. Administer IBTROZI on an empty stomach. Avoid concomitant use with strong and moderate CYP3A inhibitors and/or drugs with a known potential to prolong QTc.Hyperuricemia: Hyperuricemia can occur and was reported in 14% of patients, with 16% of these requiring urate-lowering medication without pre-existing gout or hyperuricemia. 0.3% of patients experienced Grade ≥3. Median time to first onset was 2.1 months (range: 7 days to 35.8 months). Dose interruption occurred in 0.3% of patients.Myalgia with Creatine Phosphokinase (CPK) Elevation: Myalgia with or without CPK elevation can occur. Myalgia occurred in 10% of patients. Median time to first onset was 11 days (range: 2 days to 10 months).Concurrent myalgia with increased CPK within a 7-day time period occurred in 0.9% of patients. Dose interruption occurred in 0.3% of patients with myalgia and concurrent CPK elevation.Skeletal Fractures: IBTROZI can increase the risk of fractures. ROS1 inhibitors as a class have been associated with skeletal fractures. 3.4% of patients experienced fractures, including 1.4% Grade 3. Some fractures occurred in the setting of a fall or other predisposing factors. Median time to first onset of fracture was 10.7 months (range: 26 days to 29.1 months). Dose interruption occurred in 0.3% of patients.Embryo-Fetal Toxicity: Based on literature, animal studies, and its mechanism of action, IBTROZI can cause fetal harm when administered to a pregnant woman.ADVERSE REACTIONSAmong patients who received IBTROZI, the most frequently reported adverse reactions (≥20%) were diarrhea (64%), nausea (47%), vomiting (43%), dizziness (22%), rash (22%), constipation (21%), and fatigue (20%).The most frequently reported Grade 3/4 laboratory abnormalities (≥5%) were increased ALT (13%), increased AST (10%), decreased neutrophils (5%), and increased creatine phosphokinase (5%).DRUG INTERACTIONSStrong and Moderate CYP3A Inhibitors/CYP3A Inducers and Drugs that Prolong the QTc Interval: Avoid concomitant use.Gastric Acid Reducing Agents: Avoid concomitant use with PPIs and H2 receptor antagonists. If an acid-reducing agent cannot be avoided, administer locally acting antacids at least 2 hours before or 2 hours after taking IBTROZI. OTHER CONSIDERATIONSPregnancy: Please see important information in Warnings and Precautions under Embryo-Fetal Toxicity.Lactation: Advise women not to breastfeed during treatment and for 3 weeks after the last dose.Effect on Fertility: Based on findings in animals, IBTROZI may impair fertility in males and females. The effects on animal fertility were reversible.Pediatric Use: The safety and effectiveness of IBTROZI in pediatric patients has not been established.Photosensitivity: IBTROZI can cause photosensitivity. Advise patients to minimize sun exposure and to use sun protection, including broad-spectrum sunscreen, during treatment and for at least 5 days after discontinuation. Please see accompanying full U.S. Prescribing Information.(1) Nuvation Bio Inc. IBTROZI (taletrectinib) US prescribing information. Available at: https://ibtrozipi.com/IBTROZI_taletrectinib-prescribing-information.pdf. Last accessed: March 2026(2) Wood R, Taylor-Stokes G. Cost burden associated with advanced non-small cell lung cancer in Europe and influence of disease stage. Available here. Last accessed: March 2026(3) European Lung Foundation. Lung cancer. Available here. Last accessed: March 2026(4) Patil T, Smith DE, Bunn PA Jr, et al. The incidence of brain metastases in stage IV ROS1-rearranged non-small cell lung cancer and rate of central nervous system progression on crizotinib. J Thorac Oncol. 2018;13(11):1717-1726. doi:10.1016/j.jtho.2018.07.012.(5) Drilon A, Camidge DR, Lin JJ, et al. Repotrectinib in ROS1 fusion-positive non-small-cell lung cancer. N Engl J Med. 2024;390(2):118-131. doi:10.1056/NEJMoa2302299. (6) ClinicalTrials.gov. A Study of AB-106 in Advanced NSCLC With ROS1 Fusion (NCT04395677). Available at: https://clinicaltrials.gov/study/NCT04395677 . Last accessed: March 2026(7) ClinicalTrials.gov. A single-arm Phase 2 study of taletrectinib in advanced ROS1-positive NSCLC (NCT04919811). Available at: https://clinicaltrials.gov/study/NCT04919811 . Last accessed: March 2026(8) Pérol M, A., et al. Taletrectinib in ROS1-positive non-small cell lung cancer: TRUST. Journal of Clinical Oncology, 43(16), 1920–1929. https://doi.org/10.1200/JCO-25-00275(9) Global Data. Diagnosed incident cases of non-small cell lung cancer across 8MM to reach 1.46 million in 2032, forecasts GlobalData. Available here. Last accessed: March 2026(10) Patil T, Smith DE, Bunn PA Jr, et al. The incidence of brain metastases in stage IV ROS1-rearranged non-small cell lung cancer and rate of central nervous system progression on crizotinib. J Thorac Oncol. 2018;13(11):1717-1726. doi:10.1016/j.jtho.2018.07.012.(11) Drilon A, Camidge DR, Lin JJ, et al. Repotrectinib in ROS1 fusion-positive non-small-cell lung cancer. N Engl J Med. 2024;390(2):118-131.MEDIA CONTACTSEisai Co., Ltd.Public Relations DepartmentTEL: +81 (0)3-3817-5120Nuvation Bio Inc.Kaitlyn Nealymedia@nuvationbio.comINVESTOR CONTACTSEisai Co., Ltd.Investor Relations DepartmentTEL: +81 (0) 3-3817-5122Nuvation Bio Inc.JR DeVitair@nuvationbio.comForward-Looking Statements of Nuvation Bio Inc.Certain statements included in this press release that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements are sometimes accompanied by words such as “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “should,” “would,” “plan,” “predict,” “potential,” “seem,” “seek,” “future,” “outlook” and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding taletrectinib’s therapeutic potential and the urgent need for new therapeutic options for patients with advanced ROS1+ NSCLC in Europe, our expectations that the MAA filing for taletrectinib will follow a standard review with a decision in 1H 2027 and be considered for full approval, plans for additional filings for the U.K., Canada and other regions included in Eisai’s licensed territories, and expectations for near-term disclosure of updated data. These statements are based on various assumptions, whether or not identified in this press release, and on the current expectations of the management team of Nuvation Bio and are not predictions of actual performance. These forward-looking statements are subject to a number of risks and uncertainties that may cause actual results to differ from those anticipated by the forward-looking statements, including but not limited to the challenges associated with conducting drug discovery and commercialization, and initiating or conducting clinical studies due to, among other things, difficulties or delays in the regulatory process, enrolling subjects or manufacturing or acquiring necessary products; the emergence or worsening of adverse events or other undesirable side effects; risks associated with preliminary and interim data, which may not be representative of more mature data; physician and patient behavior; and competitive developments. Risks and uncertainties facing Nuvation Bio are described more fully in its Form 10-K filed with the SEC on March 2, 2026 under the heading “Risk Factors,” and other documents that Nuvation Bio has filed or will file with the SEC. You are cautioned not to place undue reliance on the forward-looking statements, which speak only as of the date of this press release. Nuvation Bio disclaims any obligation or undertaking to update, supplement or revise any forward-looking statements contained in this press release. Copyright 2026 JCN Newswire via SeaPRwire.com. All rights reserved. www.jcnnewswire.com
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New “L00 Series” Train for the Seibu Railway’s Yamaguchi Line Begins Commercial Operation JCN Newswire

New “L00 Series” Train for the Seibu Railway’s Yamaguchi Line Begins Commercial Operation

The Frst New Leo Liner "L00 Series"TOKYO, Mar 27, 2026 - (JCN Newswire via SeaPRwire.com) - Mitsubishi Heavy Industries, Ltd. (MHI) has completed delivery of the first trainsets L00 Series ("Leo-kei") trains (4 cars per trainset, total 12 cars) ordered by Seibu Railway Co., Ltd. for its Yamaguchi Line, an automated guideway transit (AGT) system. Commercial operation of the first train began on March 27th. That same day, Seibu Railway held a commemorative ceremony for the start of commercial operation, attended by Tokorozawa City Mayor Masatoshi Onozuka and Higashimurayama City Mayor Takashi Watanabe.The new L00 Series are being manufactured at MHI's Mihara Machinery Works in Hiroshima Prefecture, and are scheduled to be delivered sequentially by FY2027. The seating arrangement has been changed from the bench seats used in the existing 8500 Series vehicles to longitudinal seats to increase transport capacity to BELLUNA DOME baseball stadium and Seibuen Amusement Park. To meet diverse passenger needs, wheelchair spaces, children's seats, and in-car information displays have been installed to enhance convenience.In addition, the new trains incorporate many unique specifications designed by MHI especially for AGT system vehicles, including aluminum bodyshells, the MHI bogie,(1), a ceiling duct air conditioning system,(2) and A-MVCS (Advanced Mitsubishi Vehicle Control System). The A-MVCS in particular, in addition to the vehicle control function, has monitoring and commissioning functions for each piece of on-board equipment, allowing it to flexibly meet the needs of railway operators.Further, a large glass window has been installed in the partition wall between the driver's cab and the children's seat, allowing children to enjoy the view from the front window and driver's seat, enhancing the sense of excitement for passengers.This AGT system utilizes rubber tires for a smooth ride and low noise. In addition, as a type of clean mobility with low CO2 emissions, the system has a reduced environmental impact, supporting the realization of a decarbonized and energy-efficient world. The adoption of vehicles that combine excellent design and environmental performance also enhances the impression of the surrounding facilities.Going forward, MHI Group will continue to strive for technological innovation, and through services that safely and comfortably transport people and goods, contribute to the development of public transport that supports the lives of people around the world.(1) A bogie developed by MHI for AGT systems. It is compatible with general rubber tire operation for AGTs.(2) A system that directs air through ducts behind the ceiling to provide air conditioning.About MHI GroupMitsubishi Heavy Industries (MHI) Group is one of the world’s leading industrial groups, spanning energy, smart infrastructure, industrial machinery, aerospace and defense. MHI Group combines cutting-edge technology with deep experience to deliver innovative, integrated solutions that help to realize a carbon neutral world, improve the quality of life and ensure a safer world. For more information, please visit www.mhi.com or follow our insights and stories on spectra.mhi.com Copyright 2026 JCN Newswire via SeaPRwire.com. All rights reserved. www.jcnnewswire.com
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Modern Dental Group Announces 2025 Annual Results, Net Profit Surges 47.7% on Digitalization-Driven Operational Efficiency Gains ACN Newswire

Modern Dental Group Announces 2025 Annual Results, Net Profit Surges 47.7% on Digitalization-Driven Operational Efficiency Gains

RESULTS HIGHLIGHTS:- The Revenue for the year ended 31 December 2025 was approximately HK$3,736.5 million, representing an increase of approximately 11.1% as compared with the same period last year.- The Gross Profit Margin for the year ended 31 December 2025 was approximately 55.8%; the gross profit was approximately HK$2,085.0 million, representing an increase of approximately 15.9% as compared with the same period last year.- The Group’s EBITDA for the year ended 31 December 2025 was approximately HK$938.1 million, representing an increase of approximately 32.4% as compared with the same period last year.- The Group’s net profit for the year ended 31 December 2025 was approximately HK$601.2 million, representing an increase of approximately 47.7% as compared with the same period last year.- Basic earnings per share for the year ended 31 December 2025 amounted to approximately HK63.7 cents, representing an increase of approximately 47.5% as compared with the same period last year.- The Board recommended the payment of a final dividend of HK15.0 cents per ordinary share for the year ended 31 December 2025.- For the year ended 31 December 2025, the Group recorded approximately 1,039,000 cases digital solution cases produced from the Group’s production facilities in Mainland China, Thailand and Vietnam, reflecting an increase of 32.7% as compared with the same period in 2024 as a result of our clients’ continued adoption of intra-oral scanners.HONG KONG, Mar 27, 2026 - (ACN Newswire via SeaPRwire.com) - 26 March 2026, Modern Dental Group Limited (“Modern Dental” or “the Group”, stock code: 03600.HK), a leading global dental prosthetic device provider, announces its annual results for the year ended 31 December 2025 (“the year”).During the year ended 31 December 2025, the Group’s multi-dimensional strategies and continuous enhancement of operational efficiency and productivity as supported by the ongoing trend of digitalization in the dental industry have resulted in the Group reporting record revenues, net profit and EBITDA numbers during this period. This occurred in a period of challenging macro-economic environment with general softness in demand for dental procedures and trade war uncertainties. The Group has been proactive in its approach to deal with the unprecedented international trade environment leveraging its international production facilities located in Thailand, Vietnam and Mainland China.The global digitalization trend continues to drive consolidation within the dental prosthetics industry, enabling the Group to further expand its market share. Our ongoing digital transformation initiatives are enhancing both customer and patient experiences while improving operational efficiency, further differentiating the Group from competitors and positioning us to outperform industry peers. The Group’s underlying fundamentals remain solid, and we are well positioned to capitalize on emerging opportunities going forward.European BusinessesDuring the year ended 31 December 2025, the European market recorded a revenue of approximately HK$1,887.0 million, representing an increase of approximately HK$268.0 million as compared with the year ended 31 December 2024. This geographic market accounted for 50.5% of the Group’s total revenue. The increase of revenue from the European market was mainly attributable to the increase in sales order volume driven by the launch of new products, such as digital dentures, and our state-of-the-art digital workflows.The Group has been the frontrunner to provide comprehensive digital solutions offerings, ranging from numerous minimal invasive and aesthetic prosthetic solutions to intra-oral scanners and clear aligners, and is well positioned to capture the opportunities arising from the accelerated digitalization trend of the dental industry. The Group continues to aggressively gain market share from international and domestic competitors through our established dental ecosystem solutions with a focus on education and digitalization, which is available within close proximity to our clients; effectively meeting our clients’ high expectations through our various onshore and offshore resources. The Group is committed and will continue to equip ourselves to provide the state-of-the-art digital solutions offerings to the dental community in the market.North American BusinessesDuring the year ended 31 December 2025, the North American market recorded a revenue of approximately HK$696.4 million, representing a decrease of approximately HK$55.7 million as compared with the year ended 31 December 2024. This geographic market accounted for approximately 18.6% of the Group’s total revenue.A significant portion of our business in the North America region comprises higher-end products manufactured domestically by MicroDental Laboratories, Inc. and its subsidiaries (“MicroDental Group”). While demand for discretionary cosmetic treatments remained soft throughout 2025, our centralized digital workflows and network-wide production oversight enabled us to deliver enhanced service quality and operational efficiencies to our North American customers.Our diversified supply bases in the US, China, Vietnam and Thailand continue to provide greater flexibility to navigate US tariff uncertainties — an advantage that sets us apart from competitors. Although digitalization of imported product lines drove growth in mass market cases, implementation of the US tariff in April 2025 introduced new uncertainties and contributed to a slow growth in sales for our import-focused business unit.Greater China BusinessesFor the year ended 31 December 2025, the Greater China market recorded a revenue of approximately HK$615.4 million, representing a decrease of approximately HK$46.8 million as compared with the year ended 31 December 2024. This geographic market accounted for approximately 16.5% of the Group’s total revenue.The Mainland China market faced headwinds from the volume-based procurement policies and a prolonged period of intense price competition and the situation started to stabilize in the second half of 2025. This also led to aggressive promotions for dental implant treatments by Mainland China dental clinics in Hong Kong (which experienced a notable decrease in patient visits in Hong Kong). The Group’s has deliberately pivoted away from low-margin segments and stay focused on serving mid- and high-value customers, ensuring long-term sustainable profitability of the Group’s business.The Group is optimistic in its mid/long-term outlook for this market in particular where the latest procurement-related government measures are expected to (i) standardize the pricing of dental prosthetics and develop price transparency, which would level the playing field; (ii) allow the Group’s leading brand name and reputation to be a key consideration for its client and customer; and (iii) have the Group benefit from its large production team and its ability to allocate resources efficiently according to the customer or client.Australian BusinessesFor the year ended 31 December 2025, the Australian market recorded a revenue of approximately HK$289.1 million, representing an increase of approximately HK$24.4 million as compared with the year ended 31 December 2024. This geographic market accounted for approximately 7.7% of the Group’s total revenue. The increase in revenue from Australia reflected a strong uptake of new digital products driven by the digitalization trend in dental industry and the revenue contribution from the acquisition of Digital Sleep which is partially offset by the depreciation of AUD against HK$ by 2.4% compared with the year ended 31 December 2024.Through our various brands, which offer onshore-and offshore-made products, at multiple price points ranging from economy and standard to premium/boutique, the Group is able to effectively penetrate the entire Australian market. We have invested in local production capacity to provide faster service to our customers, and to provide choices around where the products are made. The Group is one of the largest players in the Australian market and is a preferred supplier to the major corporate dental groups in the market.Other MarketsOther markets primarily include Thailand, Indian Ocean countries, Malaysia, Taiwan and Singapore. For the year ended 31 December 2025, these markets recorded a revenue of approximately HK$248.9 million, representing an increase of approximately HK$182.4 million as compared with the year ended 31 December 2024. This geographic market accounted for approximately 6.7% of the Group’s total revenue. The increase in revenue from Other markets was primarily driven by the revenue contribution from the newly acquired Hexa Ceram.Future Prospects and StrategiesThe global macroeconomic environment remains uncertain, with geopolitical tensions and potential tariff changes continuing to create headwinds. However, the Group’s geographically diversified production footprint and global distribution network position us strongly to navigate these challenges. Unlike many competitors reliant on single-country manufacturing, our operations across China, Vietnam and Thailand (including the newly acquired Hexa Ceram) provide superior resilience and flexibility. This strategy, combined with our ability to adapt quickly to local market conditions, enables the Group to mitigate risks and capitalize on opportunities across regions.The dental industry has continued to demonstrate remarkable resilience, underpinned by irreversible demographic trends, including aging populations and increasing awareness of oral health, which drive consistent long-term demand. Building on our record 2025 performance, the Group is well placed to sustain momentum and further strengthen its market leadership.Digitalization remains an irreversible industry trend that is accelerating consolidation of the dental prosthetics industry. We are at the forefront of this transformation, with digital solution cases now representing approximately 35–40% of total volume. Our centralized digital workflows, intra-oral scanner partnerships, proprietary solutions and global education centers have enhanced operational efficiency, reduced turnaround times and delivered superior customer experiences. These initiatives create high entry barriers and will continue to drive margin expansion and market share gains in the coming years.Following the successful integration of Hexa Ceram (Thailand’s largest dental laboratory, acquired in January 2025) and Digital Sleep Design (Proprietary nylon oral appliance to treat obstructive sleep apnea), our Southeast Asian presence and specialized capabilities have been significantly strengthened. This expansion, coupled with our diversified supply bases in the US, China, Vietnam, and Thailand, provides enhanced flexibility to address potential trade and geopolitical risks while supporting faster regional delivery.Looking ahead, the Group remains committed to reinforcing its worldwide leading position through a multi-dimensional approach. We will continue to pursue selective acquisitions, joint ventures and partnerships to expand and complement our product offerings, particularly in our high-growth clear aligner, Trioclear, while strengthening our distribution and sales networks. Ongoing investments in mass-scale production facilities, AI, automation, research and development, and digital innovation will drive efficiency gains and secure our position at the forefront of the industry.About Modern Dental GroupModern Dental Group Limited (Stock code: 03600.HK) is a leading global dental prosthetics provider, distributor and consultant with a focus on providing custom-made prostheses to customers in the growing prosthetics industry. Our product portfolio is broadly categorized into three product lines: fixed prosthetic devices, such as crowns and bridges; removable prosthetic devices, such as removable dentures; and other devices, such as orthodontic devices, sports guards, clear aligners, and anti-snoring devices. Modern Dental Group has a global portfolio of respected brands, including Labocast, Permadental and Elysee Dental in Western Europe, YZJ Dental in China, Modern Dental Lab in Hong Kong, Modern Dental USA and MicroDental in the United States, Modern Dental Pacific in Australia and New Zealand, Modern Dental SG in Singapore, Modern Dental TW in Taiwan, Apex Digital Dental in Malaysia and Hexa Ceram in Thailand. We have grown these brands by providing premium and consistent quality products and superior customer service. We have more than 80 service centers in over 28 countries and serve over 35,000 customers. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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JF SmartInvest Holdings Ltd Adjusted Profit Leaps 191.8% to RMB1.02 Billion ‘Technology + Investment Research’ Dual-Driver Strategy Delivers Remarkable Results, Overseas Expansion Ushers in a New Chapter of Globalisation ACN Newswire

JF SmartInvest Holdings Ltd Adjusted Profit Leaps 191.8% to RMB1.02 Billion ‘Technology + Investment Research’ Dual-Driver Strategy Delivers Remarkable Results, Overseas Expansion Ushers in a New Chapter of Globalisation

HIGHLIGHTS:- Total gross billings amounted to approximately RMB3,955.0 million, representing an increase of approximately 12.8% from approximately RMB3,505.9 million for the corresponding period.- Total revenue was approximately RMB3,430.1 million, representing an increase of approximately 48.7% from approximately RMB2,306.0 million for the corresponding period.- The profit attributable to Shareholders of the Group was approximately RMB921.8 million, representing an increase of approximately 238.5% from approximately RMB272.4 million for the corresponding period.- Non-HKFRS adjusted profit for the year (excluding the share-based compensation expenses) was approximately RMB1,022.5 million, representing an increase of approximately 191.8% from approximately RMB350.5 million for the corresponding period.- Taking into account the financial and cash flow positions of the Group, the Board recommends the payment of a final dividend of approximately HKD168.5 million for the year ended December 31, 2025, representing HKD0.36 per share (in cash), and the proposed final dividend is subject to consideration and approval by Shareholders at the AGM.HONG KONG, Mar 27, 2026 - (ACN Newswire via SeaPRwire.com) - JF SmartInvest Holdings Ltd (the “Company” ; together with its subsidiaries, the "Group" or “we”) is pleased to announce its consolidated annual results for the year ended December 31, 2025 (the “Reporting Period”). During the Reporting Period, leveraging its “technology + investment research” dual-drive strategy, the Group achieved outstanding performance. Supported by robust cash flow and profitability, the Board has proposed a final dividend of HK$0.36 per share, bringing the total dividend for the full year to approximately HK$407.4 million when combined with the interim dividend already paid, reflecting its commitment to delivering returns to shareholders.Strong Financial Performance with Substantial Profitability ImprovementDuring the Reporting Period, the Group continued to advance product innovation, AI applications, and investment research capabilities, driving solid growth across its business. Total revenue for the year reached RMB3,430.1 million, representing a YOY increase of 48.7%. Gross profit amounted to RMB2,821.0 million, up 48.9% YOY, while the gross profit margin remained at a high level of 82.2%, indicating the favourable economies of scale and earnings quality of the Group’s business model.In terms of profitability, profit attributable to equity shareholders surged by 238.5% YOY to RMB921.8 million. Excluding share-based compensation expenses, non-HKFRS adjusted profit for the year reached RMB1,022.5 million, representing a YOY increase of 191.8%, fully demonstrating the effective strategy execution and market adaptability of the Group.The Group places great emphasis on shareholder returns. The Board recommends the payment of a final dividend of approximately HKD168.5 million for the year ended December 31, 2025, representing HKD0.36 per share (in cash). Together with the interim dividend of approximately HK$238.9 million already distributed, the total dividend for 2025 will amount to approximately HK$407.4 million. The steady dividend policy fully reflects the Group’s ample cash reserves and its firm confidence in future development prospects.Continued Optimisation of Product Matrix and Enhancement of Diversified Service SystemDuring the Reporting Period, the Group continued to build a diversified product matrix, enriching its product portfolio in response to different customer needs. VIP products 'Stock Navigator, Super Investor' were steadily optimized, with the addition of several quantitative products and AI-powered products. We also launched a 24/7 AI intelligent customer service system, which significantly improved service efficiency. The live streaming system was upgraded, with sessions increasing by 36% YOY and average daily unique viewers exceeding 100,000.Relying on an integrated “AI + content + service + tools” solution, the Enjoy-Stock Pad recorded net sales volume exceeding 75,000 units during the Reporting Period. The Jiuyao Stocks launched over 80 lightweight products, converting professional investment research capabilities into standardised products. The SmartInvest APP completed its strategic transformation from a tool to a platform, with monthly active users increasing by more than 40% YOY and the 30-day retention rate remaining above 50%.The Group further enhanced its product matrix with two new products, Decision Master and Star-tier Services, filling the gap in the mid-tier product system and enabling a seamless trading service experience. Decision Master focuses on three AI+ investment research modules - themes, value investing and quantification - comprehensively enhances investment decision-making capabilities of individual investors. Star-tier Services collaborates with multiple securities brokerages and partners to create a fully integrated closed-loop ecosystem of“tools-services-trading”, serving over 50,000 users during the Reporting Period.Guided by Technological Innovation, Striving Towards “Investment Advisory Intelligent Agent 2.0”The Group regards innovation and technological R&D as its core driving force, accelerating its transformation towards “digital intelligence”, and advancing towards the era of “investment advisory intelligent agent 2.0”. During the Reporting Period, R&D expenses amounted to approximately RMB356 million, with R&D personnel reaching 624, a YOY increase of approximately 42.8%. The Group held 158 software copyrights and patents in AI, big data and product features, with 22 new items added on a year-on-year basis.The self-developed FinSphere Agent Large Model Assistant V3.0 passed the Large Model Assistant Functionality Completeness Test conducted by the China Academy of Information and Communications Technology, becoming the first large-model application in the securities industry. During the Reporting Period, it served approximately 664,000 customers with cumulative services of 22.58 million. The digital intelligent investment robo-advisor “Jiu Ge” served approximately 600,000 customers with cumulative services exceeding 19 million. The Group also launched stock diagnosis intelligent agent 4.0, AI Xiaoce Q&A assistant, and established an intelligent compliance and risk control platform covering the entire business workflow, indicating that the group's AI capabilities have gradually been implemented in core scenarios.To strengthen its technological foundation, the Group established a technology subsidiary, Jiufang Zhiqing, and set its foothold in “Shanghai Foundation Model Innovation Center”, China’s first large model innovation ecosystem community. The subsidiary serves as the Group’s core AI vehicle for operating a native service technology system, promoting the deep application of AI in scenarios such as investment research, investor education, and risk control.Deep-Rooted Investment Research as the Cornerstone, Adhering to Buyer-Side Advisory and Deepening the “1+N” Investment Research SystemThe Group continues to deepen its “1 research institute and N business lines” investment research system, with the JF Financial Research Institute as investment research hub. The Institute has established a pyramidal-structured professional talent echelon led by Chief Economist Dr. Xiao Lisheng, comprising 4 experts, 8 super-IPs and 128 professionals. As of the end of the Reporting Period, the Group had 576 employees holding securities investment advisory qualifications and 2,628 employees holding securities practitioners, maintains a leading team scale and structure in the industry.During the Reporting Period, The Institute conducted more than 300 research activities, covering more than 2,000 listed companies. The Institute authored approximately 1,200 in-depth research reports and 45 sets of thematic courses with a total duration of 2,000 minutes, continuously enhancing the professional capabilities of buyer-side consultants.Multi-Dimensional, Full-Funnel Traffic Operation to Unlock New Growth DimensionsDriven by AI technology, the Group positions refined MCN-based traffic operations as a central hub connecting users with its business, building an integrated, synergistic omni-channel traffic ecosystem comprising “public-domain MCN (multi-platform) + private-domain + proprietary APP”. On the technological front, the Group applied AIGC to restructure content production, shifting from manual creation to “human-machine collaboration” model, and established a data flywheel integrating “advertising data, model training and operational automation”. During the Reporting Period, the Group consolidated its leading position on online short-video and live streaming platforms’ operations, established a multi-platform coordinated traffic matrix, and developed a multi-tiered, high-quality content ecosystem. It also pioneered e-commerce models for the Enjoy-Stock Pad and AppStore models for the APP, driving deep integration between traffic operations and product features.Future OutlookMr. Chen Wenbin, chairman of the Board and chief executive officer of JF SmartInvest Holdings Ltd, said: “In 2025, we remained committed to the dual-drive strategy of ‘technology + investment research’. Not only did we achieve leapfrog growth in performance, but we also successfully led the industry into the era of ‘Investment Advisor Agent 2.0’. Leveraging artificial intelligence and big data technologies, we developed AI products such as the JF Robo-Advisor, FinSphere Agent and FinSphere Report, achieving industry-leading innovations and scenario-based applications, helping users accomplish the critical transition from ‘cognitive improvement’ to ‘decision optimisation’. At the same time, we transformed our professional investment research capabilities into easily accessible lightweight services, realising a strategic shift ‘from tool to platform’. We uphold the principles of rational investing, value investing and long-term investing, assisting clients in developing sound investment philosophies.“In the future, the Group will focus on four key strategic dimensions. First, deepening AI-driven empowerment across all scenarios, accelerating the iteration of AI agents and their commercialisation on the consumer side, and driving the Group’s digital and intelligent transformation. Second, leveraging Forthright Securities and Forthright Capital’s licenses, advancing the globalisation strategy by exporting the Jiufang’s core models, accelerating overseas business expansion. Meanwhile, promoting license upgrading and strategic investment layout to further improve the construction of digital asset infrastructure. Third, strengthening product-driven business diversification and synergies, deepening cooperation with licensed financial institutions such as securities brokerages, and building a service closed loop covering pre-investment, in-investment and post-investment. Fourth, continuing to optimize the customer operation system, unlocking the value of traffic through full-funnel traffic initiatives, and achieving long-term customer retention. We are dedicated to making investing simpler and more professional while enhancing investors’ sense of fulfillment in investment and wealth management.”About JF SmartInvest Holdings Ltd (Stock Code: 9636)JF SmartInvest Holdings Ltd is a new generation stock investment assistant. The Company is engaged in the provision of equity investment instruments, securities investment advisory, investor education and other services to individual investors. The products include stock quote software, the AI Stock Machine, Stock Navigator, Super Investor and Jiuyao Stocks. The Company adopts the technology + investment research model, develops JF Robo-Advisor, FinSphere Agent, FinSphere Report and other products based on artificial intelligence (AI) and big data technology, which are applied to the industry in terms of innovative practice and scenario application.For enquiries, please contact:Financial PR (HK) LimitedEmail: ir@financialpr.hkTel: 852 2610 0846Fax: 852 2610 0842 Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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How to Choose the Right Savings Account for Your Money Goals in Singapore ACN Newswire

How to Choose the Right Savings Account for Your Money Goals in Singapore

SINGAPORE, Mar 27, 2026 - (ACN Newswire via SeaPRwire.com) - Choosing where to place your savings in Singapore is an important financial decision that requires careful consideration. With many banks offering different types of accounts, it is easy to get confused. However, picking the right one is the first step to reaching your financial goals, whether you are saving for a dream wedding, a new home, or a retirement fund.The good news is that you no longer need to spend a whole afternoon waiting at a bank branch. You can now open a bank account online in just a few minutes using your phone or computer. Here is a simple guide to help you choose the best account for your needs in 2026.Identify Your Financial HabitsBefore focusing on interest rates, consider how you manage your money on a daily basis. Savings accounts in Singapore usually fall into two categories:The Active Saver: These accounts give you high interest rates, but you have to make a few mandatory transactions each month. Usually, you need to credit your salary and spend a set amount on your credit card.The Passive Saver: These accounts help you earn bonus interest just for keeping your money in the account and letting it grow. You do not need to worry about credit card spending or paying bills.Compare Interest RatesBefore opening a bank account online, make sure you compare the interest rates. Many basic accounts offer low interest rates. To make your money grow, you should look for bonus interest.For example, a high-interest account can offer between 2% and 5% depending on the rules you follow. If you have SGD 50,000, the difference between a basic account and a high-interest one could be hundreds of dollars in extra cash every year. Always check the effective interest rate, which tells you the real amount you will earn after all the levels are counted.Look for Welcome PromotionsBanks in Singapore are always competing for your business. When you open a bank account online, you can often grab a welcome gift, such as cash credits or rewards. These promotions are a great way to get a head start on your savings. Just make sure to check the dates, as many of these flash deals only last for a few months.Check the Fees and MinimumsEven a great account can lose you money if you are not careful about fees. Before you sign up, check for these three things:Minimum balance: Most accounts require maintaining a certain amount of money in the account at all times. If the balance drops below this limit, the bank may charge you a monthly fee.Initial deposit: Some accounts require at least SGD 1,000 to get started.ATM access: Make sure the bank has plenty of ATMs near your home or office so you do not get charged for using the machine of another bank.Open an Account OnlineOnce you have picked the right account, the final step is to fill out your application. In Singapore, you can use Singpass MyInfo to fill out your application automatically.When you open a bank account online, your details, such as your NRIC, address, and income, are pulled directly from the government database, thus reducing paperwork. Most accounts are approved almost instantly, and you can start using your new digital card right away.Final ThoughtsChoosing a savings account is not just about finding the highest interest rate. It is about finding the one that fits how you live. If you are a busy professional who already uses a credit card, an active account is perfect. If you just want to set your money aside and forget it, a passive account is better.By taking 10 minutes to compare your options today, you can ensure that every dollar you earn works as hard as you do.Disclaimer: This article is for general information only and does not have any regard to the specific investment objectives, financial situation and particular needs of any specific person. The views expressed in this article are solely those of the author. This article shall not be regarded as an offer, recommendation, solicitation or advice. You may wish to consult your own professional advisers about this article, in particular, a financial professional before making financial decisions. Any past events, trends and/or performance referred to in this article may not necessarily be indicative of future events, trends or performance. This article is based on certain assumptions and reflects prevailing conditions as at the time of publication, which are subject to change at any time without notice. The author and publisher of this article as well as any other parties associated with this article make no representation or warranty of any kind, whether express, implied or statutory, in respect of this article and accept no liability or responsibility for the completeness or accuracy of this article or any error, inaccuracy or omission relating to this article and/or any consequence, injury, loss or damage howsoever suffered by any person relating to this article, in particular, arising from any reliance by any person on this article. Publishers or platforms may be compensated for access to third party websites.Contact Information:Name: Sonakshi MurzeEmail: Sonakshi.murze@iquanti.comJob Title: ManagerSOURCE: iQuanti Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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Everest Medicines Enters into Asset Purchase Agreement for Etripamil Nasal Spray, Expanding Cardiovascular Footprint ACN Newswire

Everest Medicines Enters into Asset Purchase Agreement for Etripamil Nasal Spray, Expanding Cardiovascular Footprint

HONG KONG, March 23, 2026 - (ACN Newswire via SeaPRwire.com) - Everest Medicines today announced that it has entered into an Asset Purchase Agreement with Corxel Pharmaceuticals Hong Kong Limited ("CORXEL"). Under the agreement, the Company has acquired the rights to develop, manufacture, and commercialize CARDAMYST™ (etripamil) nasal spray in Greater China, including Chinese Mainland, Hong Kong, Macao and Taiwan region.Under the terms of the agreement, Everest will pay CORXEL an upfront payment of US$30 million (equivalent to approximately RMB344,895,000), as well as potential development milestone payments of up to US$20 million (equivalent to approximately RMB137,958,000). As part of this agreement, Everest will be assigned and transferred rights, interests, claims, duties, obligations and liabilities (other than certain excluded liabilities) under the Milestone License Agreement entered into by CORXEL in May 2021 and certain related ancillary agreements.CARDAMYST™ (etripamil) nasal spray is a novel, rapid-acting calcium channel blocker as administered as needed via a convenient, portable nasal spray. It offers rapid onset of action, favorable tolerability, and the potential for at-home self-administration, enhancing patient accessibility. In December 2025, CARDAMYST was approved by the U.S. Food and Drug Administration (FDA), becoming the first and only self-administered nasal spray in more than 30 years capable of converting paroxysmal supraventricular tachycardia (PSVT) to sinus rhythm in adults. As a rapid-acting treatment option, CARDAMYST can be self-administered outside the emergency department or other healthcare settings, enabling patients to actively manage episodes and gain greater control over their condition. In addition to its approved indication for PSVT, etripamil nasal spray is also under clinical development for atrial fibrillation with rapid ventricular response (AFib-RVR). Phase II trials have shown encouraging results, and Phase III trials are planned, with the potential to further extend its therapeutic impact to a broader patient population.In China, the New Drug Application (NDA) for etripamil nasal spray was accepted by the National Medical Products Administration (NMPA) on January 17, 2025 and is expected to receive approval in the third quarter of 2026.PSVT is characterized by abnormalities in the heart's electrical system that cause sudden unexpected and often severely symptomatic episodes of rapid heart rate. There are currently no approved self-administered, fast-acting, non-injectable therapies for acute PSVT, leaving patients with limited treatment options beyond emergency care. Approximately 2.3 to 4 per 1,000 individuals are affected by PSVT, representing an estimated 3 to 6 million patients in China.AFib-RVR is a type of irregular heart rhythm, characterized by an irregular and elevated heart rate. Its onset is typically gradual, episodes are less likely to terminate spontaneously, and the condition tends to recur, significantly increasing the risk of thromboembolism and serious complications such as stroke and heart failure. In China, atrial fibrillation affects an estimated 1.6% of the population, representing nearly 20 million patients, and is expected to increase with an aging population. Both PSVT and AFib-RVR are associated with a loss of control and a significant psychological burden for patients.Overall, the combined patient population for PSVT and AFib-RVR exceeds 25 million, representing a significantly unmet clinical need that urgently requires more convenient and more effective treatment options.In terms of clinical data, the NDA for etripamil nasal spray was accepted by the NMPA based on data from the pivotal global Phase 3 RAPID study and the China Phase 3 JX02002 study. Both trials met their primary endpoints. Overall, the treatment emergent adverse events (TEAEs) were comparable between the etripamil and placebo groups. The FDA approval of CARDAMYST was supported by a robust clinical program that included safety data from more than 1,800 participants across more than 2,000 PSVT episodes. This included the Phase 3 RAPID trial, a global, randomized, double-blind comparison of etripamil versus placebo, published in The Lancet in 2023. The RAPID trial achieved its primary endpoint, with 64% of participants who self-administered etripamil (N=99) converting from supraventricular tachycardia (SVT) to sinus rhythm within 30 minutes compared with 31% on placebo (N=85) (HR = 2.62; p
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Fujitsu develops high-sensitivity, high-resolution infrared sensor to expand monitoring capabilities in defense and disaster prevention JCN Newswire

Fujitsu develops high-sensitivity, high-resolution infrared sensor to expand monitoring capabilities in defense and disaster prevention

KAWASAKI, Japan, Mar 27, 2026 - (JCN Newswire via SeaPRwire.com) - Fujitsu today announced the development of a world-leading, high-sensitivity and high-resolution infrared sensor to expand monitoring capabilities in the defense and disaster prevention fields. This sensor is a Type-II superlattice (T2SL) infrared sensor with over 1 million pixels, capable of detecting both mid-wavelength infrared (MWIR) and long-wavelength infrared (LWIR) light. Its high-sensitivity allows it to clearly capture minute thermal differences of 0.05°C or less, enabling high-precision monitoring day and night. This over 1-megapixel dual-band T2SL infrared sensor is the first of its kind in the world.The newly developed technology boasts dramatically enhanced detection and identification performance, with applications spanning a wide range of fields. For example, when applied to optical sensor systems mounted on satellites or aircraft, it can contribute to the creation of new value across diverse areas, including early assessment of disaster situations and environmental monitoring.Integrating this sensor into monitoring devices for defense and disaster prevention enables accurate detection of thermal changes, such as identifying precursors to human activity or object movement, locating people during disasters, detecting early forest fires, and monitoring tsunamis. This contributes to improving information gathering capabilities and strengthening defense and disaster prevention. Additionally, by visualizing thermal distribution and changes over time with exceptional precision, the sensor is anticipated to play a vital role in tackling societal issues like infrastructure inspection and problems with analytical equipment, while also driving progress in scientific research.This technology was developed under contract as part of the "PROTOTYPE OF WIDE BAND AND HIGH RESPONSIVITY PHOTO-DETECTORS" from Acquisition Technology & Logistics Agency (ATLA), Japan Ministry of Defense, to which Fujitsu has completed delivery of the prototype sensor.Starting in fiscal year 2026, Fujitsu plans to leverage the manufacturing technology of this sensor to develop new products and market them for use in monitoring cameras.BackgroundIn the security sector, which underpins a safe and secure society, there is a demand for advanced sensing technologies that can detect various threats early and accurately capture their precursors. However, with the diversification of monitoring scenarios and the increasing complexity of targets, there is a need for even higher resolution sensors and improved identification capabilities through simultaneous detection of multiple wavelengths. The ATLA initiated a research prototype project to establish technology that enables target detection and identification over longer distances and wider areas than existing systems. Fujitsu, which has developed and mass-produced high-sensitivity infrared sensors, was awarded this project and has now successfully completed its development.Overview of the developed sensorInfrared sensors capture infrared radiation spontaneously emitted by objects with heat, visualizing their surface temperature distribution. Fujitsu has leveraged the characteristics of T2SL, a compound semiconductor with a superlattice structure that allows for material property control, to develop a unique dual-band sensor. The superlattice structure, where different semiconductor materials are layered at the nanometer (one billionth of a meter) level, offers high sensitivity, as well as excellent control over detection wavelengths and manufacturability. By selecting a combination of semiconductor materials with a large energy offset in their band structure (i.e., Type-II Superlattice, T2SL), it is possible to detect infrared light, which has lower energy than visible light.This sensor can detect MWIR and LWIR wavelength bands, with high-sensitivity capable of detecting temperature differences of 0.05°C or less. By simultaneously detecting two wavelengths with a single pixel, it can accurately detect and identify targets that would otherwise be obscured by background noise during detection with single-wavelength sensors. Furthermore, by advancing miniaturization of elements through the development of manufacturing processes and mounting technologies suitable for delicate T2SL materials, Fujitsu has achieved high-resolution with over 1 million pixels, enabling the capture of more distant targets.This infrared sensor, simultaneously achieving high-sensitivity, high-resolution, and dual-band detection, is suitable for monitoring applications in defense, disaster prevention, and other fields requiring high discrimination performance.Furthermore, this world-first technology from Fujitsu will drive further advancements in the sensitivity, multi-band and high-resolution capabilities of conventional infrared sensors, enabling a diverse range of product developments.Figure: Dual-band T2SL infrared sensor and example imagesAbout FujitsuFujitsu’s purpose is to make the world more sustainable by building trust in society through innovation. As the digital transformation partner of choice for customers around the globe, our 113,000 employees work to resolve some of the greatest challenges facing humanity. Our range of services and solutions draw on five key technologies: AI, Computing, Networks, Data & Security, and Converging Technologies, which we bring together to deliver sustainability transformation. Fujitsu Limited (TSE:6702) reported consolidated revenues of 3.6 trillion yen (US$23 billion) for the fiscal year ended March 31, 2025 and remains the top digital services company in Japan by market share. Find out more: global.fujitsuPress ContactsFujitsu LimitedPublic and Investor Relations DivisionInquiries Copyright 2026 JCN Newswire via SeaPRwire.com. All rights reserved. www.jcnnewswire.com
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Netflix meningkatkan harga di seluruh hiruran streaming iGame

Netflix meningkatkan harga di seluruh hiruran streaming

(AsiaGameHub) - Netflix telah menaikkan harga di seluruh jajaran streaming-nya lagi, meningkatkan biaya untuk paket iklan, paket Standar, dan paket Premium. Tarif terbaru mulai berlaku bagi anggota baru pada 26 Maret, sementara pelanggan lama akan melihat perubahan tersebut di kemudian hari. Penting untuk Diketahui Paket yang didukung iklan sekarang seharga $8,99 per bulan, naik dari $7,99. Paket Standar sekarang seharga $19,99, sementara Premium sekarang seharga $26,99. Anggota lama akan menerima email sekitar satu bulan sebelum harga baru diberlakukan pada akun mereka. Netflix Menaikkan Harga Lagi Netflix tidak meluncurkan produk baru bersamaan dengan kenaikan ini. Sebaliknya, perusahaan tersebut secara diam-diam memperbarui harga paket dan biaya anggota tambahan. Tingkat yang didukung iklan naik sebesar $1, Standar tanpa iklan naik sebesar $2, dan Premium juga naik sebesar $2. Harga anggota tambahan sekarang berada di angka $7,99 untuk paket yang didukung iklan dan $9,99 untuk paket bebas iklan. Android Authority pertama kali menyadari pembaruan harga tersebut. Netflix kemudian menyatakan bahwa perubahan ini mencerminkan investasi berkelanjutan dalam jajaran hiburan dan kualitas layanannya. Anggota baru sekarang langsung melihat tarif yang diperbarui, sementara pelanggan saat ini akan beralih ke harga yang lebih tinggi selama beberapa bulan ke depan. Perusahaan terakhir kali menaikkan harga pada Januari 2025. Sejak saat itu, Netflix terus menambahkan konten langsung dan fitur produk baru, sementara materi investornya juga menunjukkan bahwa penetapan harga merupakan bagian dari pertumbuhan pendapatan. Artikel ini disediakan oleh penyedia konten pihak ketiga. AsiaGameHub (https://asiagamehub.com/) tidak memberikan jaminan atau pernyataan apa pun terkait isinya. Kategori: Berita Terkini, Pembaruan Umum AsiaGameHub menyediakan layanan distribusi iGaming yang ditargetkan untuk perusahaan dan organisasi, dengan menghubungkan lebih dari 3.000 media premium di Asia dan lebih dari 80.000 influencer spesialis. Platform ini menjadi jembatan utama untuk distribusi konten iGaming, kasino, dan eSports di seluruh kawasan ASEAN.
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Playson Meluncurkan 4 Scarab Coins Hold and Win

(AsiaGameHub) - Playson telah meluncurkan 4 Scarab Coins Hold and Win, sebuah slot bertema Mesir baru yang dibangun dengan tambahan Mystic Feature dan pengaturan bonus yang lebih luas. Rilis ini mulai tayang pada 26 Maret dan tetap mempertahankan format Hold and Win yang familier, sekaligus menambahkan lebih banyak variasi fitur bagi operator dan pemain. Hal yang Perlu Diketahui Permainan ini menggunakan tata letak 5×3 dengan hingga empat Scarab Coins dalam satu putaran. Mystic Feature yang baru dapat mengungkapkan hingga enam sel tambahan dengan nilai koin atau jackpot. Royal Jackpot tertinggi mencapai 10.000x dari taruhan. Playson Menambahkan Lapisan Bonus Baru ke 4 Scarab Coins Perubahan utamanya adalah Mystic Feature yang baru. Red Scarab Coins dapat membuka sel tambahan selama bonus Hold and Win, sementara Violet Scarab Coins memicu Multi Feature dengan pengganda hingga 5x dan Blue Scarab Coins mengaktifkan Collect Feature yang mengumpulkan nilai-nilai yang sudah ada di lapangan. Hal ini memberikan slot tersebut pengaturan yang lebih berlapis dibandingkan permainan bonus koin standar. Royal Scarab Coin juga dapat memulai Royal Bonus Game, yang memperluas grid menjadi 5×5 dan dapat menjalankan satu atau lebih Scarab Features secara bersamaan. Dalam bonus reguler, mengisi 15 sel memberikan Grand Jackpot sebesar 3.000x. Dalam putaran Royal Bonus, mengisi ke-25 sel memberikan Royal Jackpot sebesar 10.000x. Terdapat pemicu tambahan lainnya dalam bentuk Golden Pot Feature. Saat fitur ini muncul selama salah satu permainan bonus, ia dapat berubah menjadi Scarab Coins berwarna, yang dapat memperkuat fitur yang sedang aktif atau memulai fitur lainnya. Bagi operator kasino, alur bonus berlapis seperti itu biasanya membantu menjaga durasi sesi permainan, yang jelas merupakan bagian dari strategi di balik rilis ini. Poin terakhir tersebut adalah kesimpulan berdasarkan desain permainan dan bahasa yang digunakan Playson seputar keterlibatan pemain.Anton Ivannikov, CPO di Playson, mengatakan: “4 Scarab Coins: Hold and Win mengambil performa yang telah terbukti dan menyuntikkannya dengan energi yang lebih besar melalui pengenalan Mystic Feature. Dikombinasikan dengan Royal Bonus Game yang diperluas, pemain dapat mengharapkan gameplay yang lebih kaya, momen yang lebih besar, dan potensi kemenangan yang ditingkatkan secara keseluruhan. Ini adalah contoh bagus tentang bagaimana kami terus mengembangkan judul-judul unggulan kami agar tetap kompetitif di pasar kasino online.” Artikel ini disediakan oleh penyedia konten pihak ketiga. AsiaGameHub (https://asiagamehub.com/) tidak memberikan jaminan atau pernyataan apa pun terkait isinya. Kategori: Berita Terkini, Pembaruan Umum AsiaGameHub menyediakan layanan distribusi iGaming yang ditargetkan untuk perusahaan dan organisasi, dengan menghubungkan lebih dari 3.000 media premium di Asia dan lebih dari 80.000 influencer spesialis. Platform ini menjadi jembatan utama untuk distribusi konten iGaming, kasino, dan eSports di seluruh kawasan ASEAN.
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Stakelogic Meluncurkan Candy Links Bonanza 3 Dengan Fitur Bonus Baru

(AsiaGameHub) - Stakelogic telah merilis Candy Links Bonanza 3, game ketiga dalam lini Candy Links. Slot baru ini mempertahankan fokus waralaba pada pengumpulan koin dan permainan bonus berlapis, sambil menambahkan lebih banyak aktivitas fitur seputar Hot Spots, Free Spins, dan potensi jackpot. Perusahaan mengumumkan peluncurannya pada 26 Maret. Perlu Diketahui Candy Links Bonanza 3 menggunakan 3.125 cara untuk menang. Simbol Coin mengisi panel Hurricane Links, di mana koneksi garis dapat memicu hadiah uang tunai. Free Spins dan jackpot Wheel of Fortune berada di ujung atas rangkaian bonus. Candy Links Kembali Dengan Permainan yang Lebih Didorong Koin Alih-alih mengubah arah, Stakelogic telah mempertahankan struktur inti yang membuat game Candy Links sebelumnya mudah dikenali. Candy Links Bonanza 3 masih berjalan dengan format 3.125 cara, dengan kemenangan terbentuk dari kiri ke kanan. Dari sana, fokus utama dengan cepat beralih ke simbol Coin, karena simbol-simbol ini terikat dengan panel Hurricane Links dan aliran hadiah tambahan di sekitarnya. Panel tersebut melakukan banyak pekerjaan berat. Koin yang dikumpulkan selama bermain disimpan di sana, dan ketika lima Koin terhubung secara horizontal, vertikal, atau diagonal, nilainya akan dibayarkan. Lebih dari satu kombinasi dapat mendarat dalam putaran yang sama. Karena Koin yang terkumpul tetap di tempatnya hingga fitur diatur ulang, panel menciptakan pembangunan yang stabil alih-alih sekadar hit dan hilang dalam satu putaran. Stakelogic juga telah melapisi aktivitas fitur tambahan di atas dasar itu. Hot Spots dapat muncul pada putaran apa pun, dan hadiah meningkat lebih jauh ketika Koin atau simbol khusus mendarat di dalam posisi tersebut. Simbol Rocket, Chest, dan Coin Machine juga dapat memengaruhi panel Hurricane Links dengan menambah Koin atau meningkatkan nilai koin, yang membantu mempercepat progresi. Dalam istilah slot, hal itu memberi permainan rasa momentum yang lebih jelas, terutama bagi pemain yang menyukai perkembangan fitur yang terlihat alih-alih pengulangan game dasar yang datar.Free Spins tetap menjadi bagian dari struktur dan dimulai ketika tiga atau lebih simbol Bonus mendarat. Selama putaran itu, Wild dan Multiplier dapat muncul, sementara Hot Spots menjadi lebih kuat karena dapat menggandakan simbol reguler. Kemudian ujung atas jalur fitur terbuka ke dalam Wheel of Fortune, di mana pemain dapat mendapatkan multiplier dan hadiah jackpot termasuk reward Mini, Minor, Major, dan Mega. Bagi Stakelogic, rilis ini sesuai dengan pola yang lebih luas. Studio ini terus kembali ke seri yang dikenal dan menyempurnakan lapisan mekanisnya alih-alih memulai dari nol setiap kali. Dalam arti itu, Candy Links Bonanza 3 lebih terlihat seperti pembaruan produk yang dibangun untuk menjaga format slot yang terbukti tetap aktif bagi mitra kasino dan pemain reguler, dan bukan seperti reset total. Pendekatan itu juga membantu visibilitas pencarian seputar istilah terkait seperti game slot online, slot bertema permen, slot fitur koin, slot jackpot, slot Free Spins, dan gameplay Hurricane Links. Tujuannya cukup sederhana: menjaga merek tetap familiar, tetapi memberi operator judul segar untuk ditampilkan di depan pemain. James Jelliffe, Head of Slots di Stakelogic, mengatakan: “Candy Links Bonanza telah mendapatkan tempatnya sebagai seri populer bagi kami, jadi terasa seperti waktu yang tepat untuk kembali dengan bab ketiga yang lebih besar dan cerah. Candy Links Bonanza 3 memanfaatkan pesona bermain yang dinikmati pemain tentang dunia permainan, sekaligus memberi seri ini ledakan energi segar untuk penampilan berikutnya.” Artikel ini disediakan oleh penyedia konten pihak ketiga. AsiaGameHub (https://asiagamehub.com/) tidak memberikan jaminan atau pernyataan apa pun terkait isinya. Kategori: Berita Terkini, Pembaruan Umum AsiaGameHub menyediakan layanan distribusi iGaming yang ditargetkan untuk perusahaan dan organisasi, dengan menghubungkan lebih dari 3.000 media premium di Asia dan lebih dari 80.000 influencer spesialis. Platform ini menjadi jembatan utama untuk distribusi konten iGaming, kasino, dan eSports di seluruh kawasan ASEAN.
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WSOP Kembali ke ESPN Dengan Penyiaran Langsung Acara Utama

(AsiaGameHub) - WSOP membawa Main Event-nya kembali ke ESPN pada 2026 berdasarkan perjanjian multi tahun baru. Siaran dimulai pada 2 Juli dan akan tayang di berbagai platform ESPN dengan penutupan langsung selama tiga malam di awal Agustus. Yang Perlu Diketahui ESPN akan menayangkan sekitar 100 jam pemrograman WSOP orisinal setiap tahun. Siaran Main Event dimulai dengan Day 1A pada 2 Juli. Permainan final table berhenti sejenak pada 13 Juli, kemudian dilanjutkan secara langsung dari 3 Agustus hingga 5 Agustus. ESPN Mendapatkan WSOP Kembali Dengan Rencana TV Main Event yang Lebih Besar Alih-alih menyimpan perubahan terbesar untuk akhir, WSOP membangun seluruh siaran seputar Main Event sejak tangan pertama. Di bawah kesepakatan baru, setiap hari turnamen mendapatkan setidaknya enam jam pemrograman. Itu memberi penggemar poker jauh lebih dari sekadar paket highlight. Itu juga memberi ESPN properti olahraga musim panas yang stabil dengan alur cerita harian, profil pemain, ayunan chip, kekalahan buruk, dan drama meja. Sebuah twist besar datang begitu final table terbentuk. Permainan akan berhenti pada 13 Juli, kemudian dimulai kembali 20 hari kemudian untuk final langsung pada 3, 4, dan 5 Agustus dari pukul 21.00 hingga tengah malam EST. Selama jeda itu, ESPN berencana menayangkan episode prime time yang dikurasi untuk memperkenalkan finalis dan membangun minat sebelum kartu dibagikan kembali. Bagi poker, itu berarti lebih banyak waktu untuk mengubah finalis menjadi nama yang dikenal, bukan hanya jumlah chip. WSOP juga berusaha meningkatkan kualitas produksi mendekati apa yang diharapkan penggemar dari olahraga liga besar. Omaha Productions adalah bagian dari rencana itu. Perusahaan ini dikenal atas proyek-proyek termasuk Monday Night Football dengan Peyton dan Eli, plus acara Netflix seperti Quarterback dan Receiver. Dalam istilah poker, itu bisa berarti campuran yang lebih kuat dari aksi langsung, latar belakang pemain, momen tekanan, dan penceritaan yang lebih bersih seputar final table Main Event. ESPN mengumumkan kesepakatan tersebut pada hari Kamis, sementara WSOP menyebutnya sebagai bagian dari dorongan yang lebih luas di bawah pemilik saat ini, NSUS Group.Bagi WSOP, waktu sangat penting di sini. Merek ini berganti tangan pada akhir 2024 ketika Caesars menutup penjualan hak kekayaan intelektual WSOP ke NSUS Group seharga $500 juta, sementara Ty Stewart tetap menjabat sebagai CEO. Membawa Main Event kembali ke ESPN sekarang sesuai dengan fase kepemilikan baru itu dan tujuan untuk menempatkan poker di depan audiens arus utama yang lebih luas lagi. ESPN juga memiliki sejarah dengan WSOP, yang sudah berlangsung selama beberapa dekade, sehingga jaringan ini memberi seri tersebut tanah yang familiar ditambah jangkauan yang lebih luas. Ty Stewart, CEO WSOP, mengatakan: “World Series of Poker adalah fenomena global yang melampaui kategori permainan, dan tujuan kami adalah membawanya ke audiens seluas mungkin. Kembali ke ESPN – rumah bagi momen paling ikonik kami sejak 1987 – memungkinkan kami untuk memamerkan drama kemanusiaan dari Main Event seperti belum pernah sebelumnya. Dengan komitmen pertumbuhan dari kepemilikan baru kami, ini adalah waktu yang tepat untuk membawa 'Kejuaraan Dunia' kembali ke panggung terbesar dalam olahraga.” Ashley O’Connor, Wakil Presiden, Pemrograman & Akuisisi di ESPN, mengatakan: “Kami dengan bangga menyambut World Series of Poker kembali ke ESPN. Poker dipenuhi dengan alur cerita yang tak terduga, dan tidak ada yang lebih mampu menampilkan kisah-kisah yang terbentang sepanjang turnamen selain ESPN. Membawa WSOP kembali mencerminkan komitmen berkelanjutan kami untuk menyajikan kompetisi premium yang terhubung dengan penggemar dengan cara baru dan menarik.” Dari sudut bisnis iGaming dan poker, nilainya melampaui televisi. Liputan langsung yang lebih banyak dapat meningkatkan minat pada satelit online, konten poker, kemitraan merek, dan keterlibatan lintas platform seputar WSOP Main Event. Itu juga memberi pemirsa kasual titik masuk yang lebih sederhana ke No Limit Holdem, yang masih bekerja paling baik di televisi ketika produksi membuat tekanan tumpukan, pembacaan pemain, dan titik eliminasi mudah untuk diikuti. Paparan yang lebih luas itu sejak lama penting untuk lalu lintas poker, dan WSOP jelas menginginkan efek itu lagi. Artikel ini disediakan oleh penyedia konten pihak ketiga. AsiaGameHub (https://asiagamehub.com/) tidak memberikan jaminan atau pernyataan apa pun terkait isinya. Kategori: Berita Terkini, Pembaruan Umum AsiaGameHub menyediakan layanan distribusi iGaming yang ditargetkan untuk perusahaan dan organisasi, dengan menghubungkan lebih dari 3.000 media premium di Asia dan lebih dari 80.000 influencer spesialis. Platform ini menjadi jembatan utama untuk distribusi konten iGaming, kasino, dan eSports di seluruh kawasan ASEAN.
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Policer Filipenya meningkatkan Perencanaan Agung Pinjaman Aplikasi Seni Digital yang Dilakukan Minori

(AsiaGameHub) - Polisi Nasional Filipina telah meningkatkan penegakan hukum terkait platform game online setelah peringatan baru seputar keamanan anak, kejahatan cyber, dan mekanisme mirip perjudian. Roblox telah menarik perhatian dalam upaya tersebut, meskipun polisi mengatakan penyelidikan yang lebih luas juga mencakup aplikasi game dan media sosial lainnya. Hal yang Perlu Diketahui Kepala PNP Jose Melencio Nartatez Jr memerintahkan Grup Anti-Kejahatan Cyber untuk meningkatkan tindakan terhadap aktivitas ilegal yang terkait dengan aplikasi game online. Otoritas Filipina sedang berkoordinasi dengan Departemen Teknologi Informasi dan Komunikasi serta Cybercrime Investigation and Coordinating Center. Roblox mengatakan memiliki lebih dari 111 juta pengguna aktif harian secara global, dan sekitar 40% pengguna berusia di bawah 13 tahun. Filipina Memperluas Fokus pada Risiko Roblox dan Game Online Roblox mungkin nama yang paling menarik perhatian, tetapi tindakan terbaru dari otoritas Filipina lebih luas daripada satu platform. Polisi mengatakan perilaku ilegal terkait aplikasi game sekarang membutuhkan respons kejahatan cyber yang lebih kuat, terutama di mana anak di bawah umur bisa menghadapi penggrooming, eksploitasi, atau sistem gaya perjudian yang mengaburkan batas antara bermain dan bertaruh. Kekhawatiran yang lebih luas ini penting bagi operator iGaming dan platform digital karena regulator tidak lagi memperlakukan desain game, interaksi sosial, dan keamanan anak sebagai masalah terpisah. Di Filipina, polisi mengaitkan upaya penegakan hukum saat ini dengan laporan bahwa beberapa fitur platform mungkin mengekspos anak di bawah umur ke “predasi seksual, penggrooming dan eksploitasi anak di bawah umur.” Otoritas juga menunjuk mekanisme mirip perjudian sebagai bagian dari gambaran risiko. Roblox menonjol karena skala dan audiens muda. Angka perusahaan yang dipublikasikan pada 2025 menunjukkan rata-rata pengguna aktif harian sebesar 111,8 juta, sementara sekitar 40% pengguna berusia di bawah 13 tahun pada 2024, menurut laporan perusahaan yang dikutip oleh liputan media. Bagi regulator, angka seperti itu dengan cepat meningkatkan risiko. Platform dengan banyak anak di bawah umur akan menghadapi pertanyaan yang lebih sulit ketika hadiah acak, item virtual, dan alat komunikasi sosial berada dalam ekosistem yang sama.Polisi tidak bertindak sendirian. Polisi Nasional Filipina mengatakan penyelidikan sedang berkoordinasi dengan Departemen Teknologi Informasi dan Komunikasi serta Cybercrime Investigation and Coordinating Center. Hal ini memberikan dasar penegakan hukum yang lebih luas dan menunjukkan bahwa otoritas melihat penyalahgunaan platform, eksploitasi anak online, dan kontrol keamanan digital secara bersama-sama daripada sebagai masalah terisolasi. Roblox sudah berada di bawah tekanan di pasar lain terkait keamanan anak. Pada Februari 2026, Australia eSafety mengatakan telah memberitahu Roblox tentang pengujian langsung yang terkait dengan komitmen keamanan, mengutip kekhawatiran berkelanjutan seputar penggrooming anak online dan eksploitasi seksual. Roblox juga memperkenalkan pesan yang lebih kuat dan langkah-langkah pemeriksaan usia pada akhir 2024 dan awal 2026, termasuk kontrol obrolan yang lebih ketat untuk pengguna muda dan pemeriksaan usia untuk akses obrolan. Untuk sisi perjudian dalam debat ini, titik tekanan mudah dilihat. Kritik telah lama berpendapat bahwa hadiah acak, item virtual yang bisa dibeli, dan mata uang dalam game berlapis bisa terlihat dan terasa seperti perjudian bagi anak di bawah umur, terutama ketika pengguna muda tidak sepenuhnya memahami bagaimana sistem tersebut bekerja. Kritik akademis dan kebijakan seputar mekanisme gaya loot box telah mendorong debat ini jauh melampaui kasino dan sportsbook, dan ke dalam regulasi game mainstream. Kepala PNP Jose Melencio Nartatez Jr mengatakan: “Mandat kami untuk melayani dan melindungi masyarakat sekarang mencakup cyberspace untuk menjaganya aman, terutama bagi anak-anak. Inilah yang dimaksud dengan kepolisian modern, dan PNP Anda telah tetap up-to-date.” Artikel ini disediakan oleh penyedia konten pihak ketiga. AsiaGameHub (https://asiagamehub.com/) tidak memberikan jaminan atau pernyataan apa pun terkait isinya. Kategori: Berita Terkini, Pembaruan Umum AsiaGameHub menyediakan layanan distribusi iGaming yang ditargetkan untuk perusahaan dan organisasi, dengan menghubungkan lebih dari 3.000 media premium di Asia dan lebih dari 80.000 influencer spesialis. Platform ini menjadi jembatan utama untuk distribusi konten iGaming, kasino, dan eSports di seluruh kawasan ASEAN.
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Hua Medicine Announces 2025 Annual Results ACN Newswire

Hua Medicine Announces 2025 Annual Results

- Annual sales of HuaTangNing exceeded 4 million packs, a year-on-year increase of 91%, with revenues reaching RMB 492.9 million, a year-on-year increase of 93%, marking outstanding results from the Company’s fully independent commercialization operation.- Delivered record financial performance, with profit before tax reaching RMB 1,106.4 million; maintained a robust bank balance and cash position of RMB 1,092.3 million at year-end, laying a solid foundation for sustainable operations and growth.- Gross margins rose to 56.9%, and selling expenses as a percentage of revenue were optimized to 33.6% from 59.9%, significantly enhancing profitability.- HuaTangNing renewed its listing in the new National Reimbursement Drug List (NRDL) at the same price in 2025 for the calendar years 2026 and 2027, reaffirming its clinical and innovative value.- With the approval of PTE, market exclusivity in China granted another 5 years to April 2034, further strengthening commercial certainty.- Dorzagliatin was approved for commercialization in Hong Kong as HYHOMSIS®, accelerating its global expansion toward South-East Asia.- Multiple real-world evidence published to demonstrate therapeutic advantage of dorzagliatin.- Continuous expansion of therapeutic potential of glucose homeostasis and initiation of new first-in-disease indications study covering diabetes prevention, rare diseases, mild cognition impairment and frailty.SHANGHAI, Mar 27, 2026 - (ACN Newswire via SeaPRwire.com) – Hua Medicine ("the Company", Hong Kong Stock Exchange Stock Code: 2552) announces the audited consolidated results of the Company and its subsidiaries for the year ended December 31, 2025 (the “Reporting Period”). During the Reporting Period, the commercialization of HuaTangNing (dorzagliatin tablets), the Company’s core product – the global first-in-class innovative anti-diabetes medicine, glucokinase activator (GKA) – advanced comprehensively across all fronts, the Company’s independent commercialization team was efficiently and seamlessly established in its first year of operations, the Company’s R&D pipeline continued to be enriched, and the Company’s financial performance achieved a historic breakthrough, successfully entering a new stage of profitability, injecting strong momentum into the innovative development of the global diabetes treatment field.Dr. Li CHEN, Founder and CEO of Hua Medicine, stated: “2025 is a remarkable year in the commercialization operation of Hua Medicine. The Company has successfully advanced from R&D to commercialization driven organization and achieved the fully independent capacity in commercialization of global first in class novel glucose homeostasis regulator HuaTangNing. With strong market execution and product competitiveness, we have achieved nearly triple-digit growth in sales volume and revenue over 2024 when the commercialization was farmed out to sales and marketing partners. At the same time, the Company has made key progress in global market expansion through registration of drozagliatin in Hong Kong and position it toward 700 M population in south-east Asia. We continue to expand the clinical application of glucose homeostasis regulation technology and engage in new indications such as early-stage Alzheimer’s disease and Frailty. The first-in-disease efforts in GCK-MODY and Frailty set the new innovation course of Hua Medicine in the next 5 years.” Business Highlights and Operational Progress- Fully Powered Commercialization, Historic Breakthrough in ProfitabilityOn January 1, 2025, the Company assumed full responsibility for the commercialization of HuaTangNing, allowing the company to consolidate both operational and strategic control over market execution in China. The Company successfully built a professional sales team covering 10 sales regions around the country, focusing on marketing, medical affairs and commercial operation. Through an AI-empowered digital commercialization platform, operational efficiency and sales productivity were greatly enhanced, injecting new vitality into the Company’s commercial development.Reimbursement coverage under the NRDL has significantly increased accessibility, especially in Tier 2 and Tier 3 hospitals, and played a critical role in accelerating patient adoption. Since its launch in October 2022, HuaTangNing has been prescribed to over 500,000 patients through 3,000+ hospitals, community centers, pharmacies and online channels.Sales performance exceeded expectations, with 4.011 million packs of HuaTangNing sold during the reporting period, representing a 91% increase over the fiscal year 2024. This growth was achieved at the same price for both periods, underscoring strong demand and successful execution of Hua’s commercial strategy.In terms of profitability, the Company’s gross profit reached approximately RMB280.4 million, a year-on-year increase of 125%. Thanks to expanded production scale and optimized manufacturing processes, the Company’s gross margin improved to 56.9%, increasing by 8.2 percentage points as compared to 48.7% for the year of 2024. Selling expenses increased only by RMB12.3 million to RMB165.5 million, reflecting a significant positive trend towards profitability when our selling expenses in the 2025 fiscal year represents only 33.6% of revenue, whereas in the 2024 fiscal year, our selling expenses represented approximately 59.9% of revenue. In fiscal year 2025, our commercialization efforts achieved profits of approximately RMB114.9 million (as defined by gross profits less selling expenses). Although we expect to continue to increase personnel to our commercialization team, we expect this profitability trend in our commercial operations in mainland China to continue.Following the termination of the collaboration with Bayer at the end of 2024, dorzagliatin achieved a record-high sales volume. Profit before tax increased to RMB1,106.4 million for the fiscal year 2025. We ended fiscal year 2025 with a cash position of approximately RMB1,092.3 million.- Accelerated Global Layout, Strengthened Core Rights and InterestsThe Company took a key step in global expansion. On February 27, 2026, dorzagliatin (trade name: MYHOMSIS®, was successfully approved for marketing by the Hong Kong regulatory authority. The Company plans to officially launch the product in the Hong Kong market by the middle of 2026 and further expand to Asian regions. In addition, the Company submitted a new drug registration application in Macau in 2025.The Company also made new progress in intellectual property protection. In February 2026, the patent term extension (PTE) application for dorzagliatin was formally approved by the China National Intellectual Property Administration, thereby the core patent protection period of dorzagliatin extended to April 2034 and an additional 5-year market exclusivity obtained, which provides a strong guarantee for the product’s long-term market competition.In 2025, dorzagliatin was recognized as national innovation and an effective therapy for chronic diseases by the regulatory authorities in China. Accordingly, the same NRDL price was offered for the calendar years 2026 and 2027. Reimbursement coverage under the NRDL has significantly increased accessibility, especially in Tier 2 and Tier 3 hospitals, and played a critical role in accelerating patient adoption. The Company will continue to safeguard the product’s market competitiveness and patient accessibility and accelerate the popularization of the drug among patients.- Advancement of Real-World Studies, Continuous Validation of Clinical ValueReal-world evidence (RWE) studies continue to corroborate the key role of dorzagliatin in improving glucose-dependent pancreatic islet secretion function, and demonstrate its efficacy in diabetes prevention, remission, and delaying or preventing diabetes complications.The RWE study sponsored by Hua Medicine HMM0701 with 380 T2D patients was fully enrolled in 2025. The interim analysis, as reported at the 2025 American Diabetes Association (ADA), showed that 86% of such patients were taking two or more antidiabetic drugs and 41% of such patients were using insulin. After a 6-month treatment, a significant improvement of glycemic control was observed with HbA1c reduction from 8.1% to 7.3% with the mean time-in-range (TIR) levels increasing to over 70%. Thus far, the studies have demonstrated that when dorzagliatin is administered in combination with other antidiabetic drugs, such patients have experienced significantly improved post-meal glucose levels and improved β-cell function.Separately, a mechanistic study with dorzagliatin (employing double-tracer measurement) was conducted in the United States to provide scientific evidence of hepatic glycogen formation in T2D patients with an average of 17 years of diagnosed diabetes. In this study, patients were treated with dorzagliatin twice daily for 6 weeks. The results showed that dorzagliatin increased direct glucose flux to hepatic glycogen implying the improvement of restoration of hepatic Glucokinase (GK) function. Together with the clinical research data that dorzagliatin improves early phase insulin release and GLP-1 secretion, recovery of hepatic glycogen synthesis in T2D patients offers an important path in controlling post-meal glucose excursion and provides a unique opportunity in controlling diabetes complications, such as diabetes kidney diseases and mild cognition impairment.The RWE sponsored by Hua Medicine (HMM0601) has completed clinical trials with over 2,000 subjects, with average diabetes duration of 7.9 years and above 30% having disease duration more than 10 years. The initial results suggest that dorzagliatin is safe and well tolerated in Chinese T2DM patients. There were no new adverse effects observed in the study and the incident rate remains as low as what was observed in Phase III clinical trials. Patient adherence was generally high, with a mean adherence rate of approximately 95%. In this study, 80% of the participants have used one or more oral anti-diabetes medicine, and 20% used insulin. Dorzagliatin demonstrated good efficacy and safety not only in the overall population but also in elderly, obese, and hyperglycemic patient populations, whether used as monotherapy or in combination with metformin, SGLT2 inhibitors, insulin, and other medications. The topline results will be reported at the 2026 American Diabetes Association.- Deepened Clinical R&D, Continuous Expansion of New IndicationsNew Indication for Dorzagliatin – MODY-2 Patients.Medical experts in mainland China and Hong Kong have conducted independent clinical and preclinical studies of dorzagliatin for MODY-2 treatment. MODY-2, also called GCK-MODY, is a monogenic disease in which patients have a genetic defect of glucokinase gene (GCK) which results in elevated blood glucose and significant reduction of the second phase insulin secretion. The population of GCK-MODY patients is approximately 1.7 million in China. These patients are diagnosed with diabetes at a young age and represent an unmet medical need given that currently available medications are not effective. In clinical studies with MODY-2 patients, China investigators have reported that dorzagliatin is effective in reducing blood glucose levels to normal levels in MODY-2 patients who previously failed to manage their elevated blood glucose levels when treated with metformin, TZD, DPP-IV inhibitors, and SGLT-2 inhibitors. Additional results demonstrated that a single dose of dorzagliatin improved overall glucose sensitivity and second phase insulin secretion significantly in GCK-MODY patients, suggesting a unique mechanism of action of dorzagliatin to regulate GLP-1 secretion. Based on such results, Hua Medicine has communicated and reached a consensus with the CDE at NMPA to file the IND submission of dorzagliatin for MODY-2 patients in 2026.Dorzagliatin for Diabetes Prevention.Prevention of diabetes is an important focus at Hua Medicine. There are approximately 1.12 billion people living with prediabetes worldwide. We have initiated SENSITIZE 3 clinical study in Hong Kong in pre-diabetic (IGT) subjects and in early diabetes patients. These studies represent first-in-disease studies. In this double-blinded placebo-controlled study, we will evaluate the blood glucose management and pancreatic function under IVGTT and OGTT conditions to better define the clinical treatment baseline and endpoints. We expect to complete this study in 2026 and explore the opportunity to file IND applications of dorzagliatin for diabetes prevention in China and Asian Pacific regions thereafter. Dorzagliatin for Neurodegenerative Diseases.MCI shows approximately 15.5% prevalence among elderly people in China and approximately 22% in the US, and is common in T2D patients with a 45% incidence rate. The development of dorzagliatin for neurodegenerative disease is a new focus in our drug discovery efforts. Through the Genome-Wide Association Study (GWAS) and Mendelian Randomization (MR) study, we have realized the important role of GCK gene activation in the prevention of memory loss and cognitive impairment in humans. It has also come to our attention that post-meal glucose excursion is closely related to Alzheimer disease and dementia. The bio-energy balance in the brain is largely dependent on the glucose homeostasis control in the peripheral organ and the neural network communication in the central and peripheral system via spatial temporal management. Impaired glucose homeostasis and diabetes conditions result in a reduction of glucose transporter expression and insulin receptor expression in the brain, which can be prevented by low dose dorzagliatin. We have realized the potential of dorzagliatin in the treatment of mild cognitive impairment (MCI) and will initiate these first-in-disease clinical studies in the future.Dorzagliatin for Frailty.Frailty is an age-related geriatric syndrome characterized by reduced tolerance to internal and external stressors. Approximately 17% of Americans and 11% of Asians over the age of 50 suffer from frailty, while pre-frailty affects roughly 50% and 47% of these populations, respectively. It is not a single-organ disease, but the consequence of dysregulated multisystem homeostasis. Genetic evidence supports the causal effects of glucokinase (GK) activation on lowering frailty risk. We plan to initiate clinical studies in the future to advance dorzagliatin’s application in frailty.Development of combination therapy for diabetes and complications.Dorzagliatin rescues pancreatic function in glucose insulin secretion and GLP-1 secretion, as evidenced by clinical and basic research results. It also improves hepatic insulin sensitivity and reduces hepatic insulin resistance through recovery of hepatic glycogen synthesis in T2D patients. The combination of dorzagliatin with DPP-IV inhibitors, SGLT-2 inhibitors, and GLP-1 agonists have demonstrated effective regulation of lipid metabolism. Studies in combination with anticancer PI3K inhibitors have also offered unique benefits for glucose homeostasis management.- Diversified Product Pipeline, Innovative Layout for Future GrowthHua Medicine continues to enrich its pipeline layout based on core products. The Company has accelerated the R&D of a fixed-dose combination (FDC) of dorzagliatin and metformin as a twice-daily therapy for Type 2 diabetes patients with inadequate glycemic control on metformin alone, to further improve patient medication compliance. The product is supported by the strong results of the loose-dose combination in both Phase III clinical trials and real-world use. The Company has submitted an IND application to NMPA, and the GMP commercial manufacturing process has been successfully carried out, preparing for the pivotal bioequivalence study for NDA filing in 2027. Clinical studies have shown that the combination of dorzagliatin and metformin can better control blood glucose, reduce postprandial blood glucose and improve fasting blood glucose, providing new clinical value for optimizing blood glucose homeostasis endpoints.We have advanced our 2nd generation GKA as a once daily therapy for patients with obesity, leveraging dorzagliatin effects in improved glucose-stimulated GLP-1 secretion in the pancreas and in the intestine. The MAD study of the 2nd generation GKA was initiated in the United States with first-patient-in in December 2025, and we expect to report topline data by the middle of 2026.Meanwhile, the Company is also exploring combination therapy regimens of dorzagliatin with GLP-1 receptor agonists, SGLT-2 inhibitors and other drugs. In a recently published clinical trial in China, researchers reported the superior benefits of our dorzagliatin in combination with semaglutide as compared to semaglutide alone in a 12-week study. The combination group showed superior results across several key measures, including glycemic control, bodyweight related indicators and β-cell function.Financial Summary- Revenue generated by the Company was approximately RMB 492.9 million from the sale of approximately 4.011 million packs of HuaTangNing, increases of approximately 93% and 91% respectively, as compared with the year ended December 31, 2024.- Gross profit generated by the Company for the year ended December 31, 2025, was approximately RMB280.4 million, representing an increase of approximately 125%, as compared with the year ended December 31, 2024, and gross margins rose to 56.9%.- Profit before tax increased by approximately 542% to approximately RMB1,106.4 million for the year ended December 31, 2025, as compared with the year ended December 31, 2024.- Bank balances and cash position was approximately RMB1,092.3 million as of December 31, 2025.- Expenditures incurred by the Company for the year ended December 31, 2025, were approximately RMB433.4 million.Forward-Looking StatementsThis document contains statements regarding Hua Medicine's and its products' future expectations, plans and prospects. Such forward-looking statements relate only to events or information as of the date on which the statements are made in this document and are subject to change in light of future developments. Except as required by law, the Company shall not be obligated to update or publicly revise any forward-looking statements or unforeseen events after the date of such statements, whether as a result of new information, future events or other circumstances. Please read this document carefully and understand that actual future performance or results of the Company may differ materially from expectations due to various risks, uncertainties or other statutory requirements.About Hua MedicineHua Medicine (The “Company”) is an innovative drug development and commercialization company based in Shanghai, China, with companies in the United States and Hong Kong. Hua Medicine focuses on developing novel therapies for patients with unmet medical needs worldwide. Based on global resources, Hua Medicine teams up with global high-calibre people to develop breakthrough technologies and products, which contribute to innovation in diabetes care. Hua Medicine's cornerstone product HuaTangNing (dorzagliatin tablets), targets the glucose sensor glucokinase, restores glucose sensitivity in T2D patients, and stabilizes imbalances in blood glucose levels in patients. HuaTangNing was approved by the National Medical Products Administration (NMPA) of China on September 30th, 2022. It can be used alone or in combination with metformin for adult T2D patients. For patients with chronic kidney disease (CKD), no dose adjustment is required. It is an oral hypoglycemic drug that can be used for patients with Type 2 diabetes with renal function impairment. In February 2026, dorzagliatin (Trade name: MYHOMSIS®,) was approved for marketing by the Pharmaceutical Services of the Department of Health of the Government of the Hong Kong Special Administrative Region of China.For more informationHua MedicineWebsite: www.huamedicine.comInvestorsEmail: ir@huamedicine.comMediaEmail: pr@huamedicine.com Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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Unisound Posts Strong First Annual Results Since Listing: Revenue Surges Nearly 30%, H2 Loss Narrows Significantly by Over 90%, Profitability in Sight, Charting a New Course in Native Agentic AI! ACN Newswire

Unisound Posts Strong First Annual Results Since Listing: Revenue Surges Nearly 30%, H2 Loss Narrows Significantly by Over 90%, Profitability in Sight, Charting a New Course in Native Agentic AI!

HONG KONG, Mar 27, 2026 - (ACN Newswire via SeaPRwire.com) – 26 March, Unisound (09678.HK) announced its audited annual results for the year ended December 31, 2025. As the Company's first annual results announcement since listing, it underscores strong growth momentum and continued improvement in its financial profile.Revenue Mix Continues to Improve, with Faster Growth in H2For the full year of 2025, Unisound achieved total revenue of $175 million, representing a year-on-year (YoY) increase of 29%. Revenue in the second half of the year increased by 33% YoY to $117 million.It is worth noting that the Company's large language model (LLM) business generated a full-year revenue of $88.43 million, surging by over 10 times YoY. In particular, this business contributed approximately $72.49 million in H2 revenue, five times the level recorded in H1, demonstrating a compelling capacity for large-scale commercial application.Losses Narrowed Significantly, Making the Path to Profitability Increasingly ClearAlongside the rapid revenue growth, the Company's losses improved markedly. In the second half of 2025, the Company's net loss narrowed by 84% YoY, and its adjusted loss narrowed by 92% YoY, approaching break-even. This reflects the Company's ongoing improvements in cost control and operational efficiency.Simultaneously, some of the Company's operating metrics saw marked improvement. The adjusted expense ratio declined significantly by 10 percentage points YoY, while selling expenses decreased rather than increased and accounted for only 5.4%, highlighting a clear improvement in cost-to-efficiency ratio. In 2025, revenue per employee reached $365,300, up 25% YoY from $292,900 in 2024. Employee productivity continued to lead the industry, clearly underscoring the Company's core strengths in technology-driven, lean operations.Dual-Engine Strategy Gains Traction, with AI in Healthcare and AI in Daily Life Advancing in TandemIn 2025, driven by both technological breakthroughs and policy tailwinds, global demand for AI continued to rise. Unisound adhered to its "Strong Foundation Model + Deep Application" strategy, continued to strengthen its multimodal technology foundation, and drove the continuous elevation of the global influence of its proprietary large model matrix in fields such as healthcare, speech, and OCR.On the commercialization front, the Company leveraged its AI-native organization to accelerate business execution, and its dual-engine strategy in AI in Healthcare and AI in Daily Life delivered notable results. During the reporting period:The AI in Daily Life business achieved revenue of $140 million, a YoY increase of 30.8%. Among this, the Transportation segment recorded nearly 40% YoY growth. At present, AI agent applications based on the Shanhai large model have been deployed in more than 10 cities, including Qingdao, Ningbo, Shenzhen and Nanning. In addition, cumulative AI chip shipments exceeded 110 million units, further validating the Company's scale capabilities in endpoint AI products.The AI in Healthcare business achieved revenue of $35.38 million, a YoY increase of 22.3%, with average revenue per customer growing by 53.2% YoY. In 2025, over 70% of the hospitals the Company collaborated with were tertiary hospitals, and more than one-third of customers had maintained continuous cooperation for over three years. The medical-record entry and generation products powered by the medical large model delivered a 10-fold YoY increase in full-annual medical record generation at a single campus of a leading Class III hospital. The commercial insurance AI agent platform recorded a 37-fold YoY increase in case processing volume. In deep cooperation with a leading insurance group, the expense control rate was effectively raised to approximately 20%, delivering more than $145 million in incremental cost management compared with traditional review methods, comprehensively empowering insurance institutions to refine their medical risk management operations.Continued R&D Investment Strengthens the Technology MoatTo consolidate its industry-leading position, the Company continued to invest heavily in R&D in 2025. Full-year R&D expenses exceeded $55.09 million, accounting for 75% of the Company's adjusted operating expenses, while R&D personnel accounted for 69% of the total workforce. This sustained investment drove breakthroughs across multiple technology areas. For example, in the MedBench 4.0 evaluation, the Company ranked first place in three technical paradigms: "Medical AI Agent," "Medical Large Language Model," and "Medical Multimodal Large Model," earning a "Triple Crown."Outlook: Deepening the Technological Foundation and Expanding Application BoundariesLooking ahead, Unisound will continue to deepen its "Strong Foundation Model + Deep Application" strategy. On the technological front, the Company will continue to increase strategic investment in foundational large models and strive to maintain a world-class level. On the application front, it will use the large-scale expansion of MaaS (Model-as-a-Service) and AI agents as its core growth engine, driving exponential growth in its AI in Daily Life and AI in Healthcare businesses. Meanwhile, the Company is actively exploring the establishment of a recurring revenue system through models such as API calls and Token-based billing, and regards opportunities in consumer-facing (C-end) products as a second growth curve to further expand its commercialization boundaries.Between Q2 and Q3 2026, Unisound will launch a native AI agent large model for programming and office applications, which is expected to double both intelligence density and token production efficiency. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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Mengapa Menyewa Tukang Lanskap Dublin untuk Taman Anda

(SeaPRwire) - Temukan bagaimana Premier Gardens mengubah ruang luar dengan tukang kebun lanskap dublin ahli dan layanan perawatan taman Dublin yang disesuaikan untuk keindahan, fungsionalitas, dan hasil yang tahan lama.Dublin, Irlandia 25 Mar 2026 - Premier Gardens dengan bangga memperkenalkan layanan tukang kebun lanskap dublin ahli dan perawatan taman Dublin, yang dirancang untuk meningkatkan ruang luar di seluruh kota. Seiring pemilik rumah semakin mencari bantuan profesional untuk meningkatkan taman mereka, Premier Gardens menonjol dengan memberikan solusi lanskap berkualitas tinggi, andal, dan kreatif. Taman yang terawat baik tidak hanya meningkatkan daya tarik estetika properti tetapi juga menambah nilai dan fungsionalitas. Dengan tukang kebun lanskap dublin dan perawatan taman Dublin, Premier Gardens menawarkan rangkaian layanan lengkap, mulai dari desain taman dan penanaman hingga pemeliharaan rutin dan perawatan musiman. Tim terampil mereka memastikan setiap proyek ditangani dengan presisi dan perhatian terhadap detail. Memilih tukang kebun lanskap dublin dan perawatan taman Dublin berarti berinvestasi dalam keahlian dan hasil jangka panjang. Premier Gardens menggabungkan desain inovatif dengan solusi praktis, memastikan taman tetap indah dan mudah dirawat sepanjang tahun. Baik itu taman perumahan kecil atau ruang luar yang luas, para profesional mereka membawa kreativitas dan efisiensi ke setiap tugas. Yang membedakan Premier Gardens adalah pendekatan yang berfokus pada pelanggan. Layanan tukang kebun lanskap dublin dan perawatan taman Dublin mereka disesuaikan untuk memenuhi kebutuhan unik setiap klien. Mulai dari perawatan halaman dan pemangkasan pagar hingga transformasi lanskap lengkap, mereka menyediakan opsi fleksibel yang sesuai dengan anggaran dan preferensi yang berbeda. Keberlanjutan juga merupakan prioritas utama bagi Premier Gardens. Dengan menggunakan praktik ramah lingkungan dan bahan berkualitas tinggi, layanan tukang kebun lanskap dublin dan perawatan taman Dublin mereka mempromosikan lingkungan luar ruangan yang lebih hijau dan sehat sambil mengurangi dampak lingkungan. Dengan reputasi keunggulan yang kuat, Premier Gardens telah menjadi pilihan tepercaya bagi pemilik rumah yang mencari solusi lanskap yang dapat diandalkan. Komitmen mereka terhadap kualitas, profesionalisme, dan kepuasan pelanggan memastikan setiap taman yang mereka kerjakan mencapai potensi penuhnya. Ubah ruang luar Anda hari ini dengan Premier Gardens dan rasakan manfaat dari layanan tukang kebun lanskap dublin ahli dan perawatan taman Dublin yang benar-benar membuat perbedaan. Hubungi Kami Premier Gardens Dublin, Irlandia 851613673 info@premiergardens.ie https://premiergardens.ieKontak MediaPremier Gardensinfo@premiergardens.ie851613673https://premiergardens.ie Sumber :Premier GardensArtikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Arun Kumar Mengkonsolidasi Interests Global untuk Mendorong Ekosistem Multi-Sektor Terpadu di bawah AR Holdings

(SeaPRwire) - Membangun struktur terpadu yang berbasis di AS untuk meningkatkan penyelarasan operasional, standar tata kelola, dan skalabilitas jangka panjang di berbagai sektor bisnis global.Mountain View, California 26 Mar 2026 - AR Holdings Group Corporation hari ini mengumumkan konsolidasi kepentingan bisnis globalnya di bawah struktur induk terpadu yang berbasis di AS, menandai langkah kunci dalam strategi jangka panjangnya untuk membangun ekosistem multi-sektor yang terintegrasi di seluruh industri teknologi, infrastruktur, keuangan, dan konsumen. Berkantor pusat di 1075 Terra Bella Ave, Mountain View, CA, AR Holdings Group Corporation menyatukan portofolio perusahaan yang beragam yang beroperasi di berbagai sektor, termasuk infrastruktur digital, blockchain, kecerdasan buatan, telekomunikasi, perbankan, konstruksi, logistik, elektronik konsumen, dan merek gaya hidup. Konsolidasi ini mencerminkan fokus Grup dalam menciptakan kerangka kerja operasional yang kohesif yang meningkatkan koordinasi antar unit bisnisnya sekaligus mendukung pertumbuhan yang terukur di pasar internasional. Model AR Holdings berpusat pada integrasi—di mana setiap vertikal bisnis dirancang untuk saling melengkapi dan memperkuat satu sama lain. Dengan menyelaraskan platform digital dengan infrastruktur fisik dan industri yang berhadapan dengan konsumen, Grup ini bertujuan untuk menciptakan sistem yang efisien dan saling terhubung yang mampu memberikan nilai jangka panjang. Bidang pengembangan utama dalam Grup ini mencakup kemajuan dalam infrastruktur blockchain, komputasi yang berfokus pada privasi, aplikasi kecerdasan buatan, sistem keuangan, telekomunikasi, dan proyek infrastruktur berkelanjutan. Arun Kumar, Pendiri AR Holdings Group Corporation, adalah seorang pemimpin visioner dengan pengalaman lebih dari 15 tahun di bidang teknologi SDM dan inovasi blockchain. Ia telah memainkan peran kunci dalam mengembangkan sistem yang mengubah cara organisasi mengelola talenta dan mengadopsi teknologi baru. Sebagai pendiri, pandangan jauh ke depan dan pendekatan kewirausahaan Arun Kumar telah meletakkan dasar bagi organisasi multi-industri yang dirancang untuk skalabilitas jangka panjang. Fokusnya pada eksekusi, ketahanan, dan pemikiran terintegrasi terus memandu arah strategis Grup. "AR Holdings dibangun di atas keyakinan bahwa masa depan terletak pada sistem yang terhubung, bukan bisnis yang terisolasi," kata Arun Kumar. "Konsolidasi ini memperkuat kemampuan kami untuk berkembang secara global, beroperasi secara efisien, dan terus membangun di berbagai industri dengan perspektif jangka panjang." Portofolio Grup mencakup berbagai sektor, termasuk platform teknologi, layanan keuangan, solusi telekomunikasi, elektronik konsumen, pengembangan infrastruktur, operasi logistik, dan merek konsumen. Selain itu, AR Holdings mendukung inisiatif dampak sosial melalui yayasannya, yang berfokus pada kehidupan berkelanjutan, pengembangan masyarakat, dan penelitian. Dengan strukturnya yang berbasis di AS, AR Holdings memperkuat komitmennya untuk beroperasi dalam kerangka peraturan yang ditetapkan sambil memperluas jejak globalnya. Grup ini terus memprioritaskan tata kelola, transparansi, dan kepatuhan saat membangun kemitraan dengan institusi, bisnis, dan pemangku kepentingan sektor publik. Tentang AR Holdings Group Corporation AR Holdings Group Corporation adalah organisasi terdiversifikasi yang membangun bisnis terintegrasi di seluruh sektor teknologi, infrastruktur, keuangan, dan konsumen. Melalui pendekatan berbasis ekosistem, Grup ini berfokus pada pengembangan sistem yang terukur dan saling terhubung yang mendukung inovasi, pertumbuhan ekonomi, dan penciptaan nilai jangka panjang. Untuk informasi lebih lanjut, kunjungi: https://thearholdings.group Kontak Media AR Holdings Group Corporation Email: info@thearholdings.groupKontak MediaAR Holdings Group Corporation1arholdingsgroup@gmail.com1075 Terra Bella Ave, Mountain View CA 94043https://thearholdings.group Sumber : AR Holdings Group Corporation Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Atua AI Maju Alat Pengembangan AI untuk Produktivitas Web4

(SeaPRwire) - Platform AI terdesentralisasi meningkatkan perangkat alat AI-native untuk mendukung otomatisasi alur kerja cerdas dan pengembangan di seluruh lingkungan multirantai.Singapura, Singapura 25 Mar 2026 - Atua AI, platform kecerdasan buatan terdesentralisasi yang berfokus pada produktivitas dan pengembangan di ekosistem blockchain, telah mengembangkan perangkat alat pengembangan AI-native untuk meningkatkan efisiensi alur kerja dan otomatisasi di seluruh lingkungan terdesentralisasi. Perangkat alat platform ini dirancang untuk membantu pengembang, kreator, dan perusahaan menyederhanakan proses yang terlibat dalam pembangunan dan pengelolaan aplikasi terdesentralisasi. Alat AI-native termasuk Chat, Writer, Coder, dan Classifier terintegrasi ke dalam sistem terpadu yang memungkinkan pengguna menangani tugas seperti pembuatan konten, pengkodean, analisis, dan koordinasi alur kerja. Alat ini beroperasi dalam kerangka kerja cerdas yang mendukung otomatisasi sekaligus memungkinkan pengguna mengelola proses pengembangan yang kompleks dengan lebih efektif. Atua AI mendukung penerapan multirantai di seluruh jaringan blockchain seperti Ethereum, BNB Chain, dan XRP Ledger. Kompatibilitas ini memungkinkan pengguna mengintegrasikan alat bertenaga AI ke dalam aplikasi terdesentralisasi sambil mempertahankan interoperabilitas di seluruh ekosistem terdistribusi. J. King Kasr, Kepala Ilmiah di KaJ Labs, menekankan bahwa alat pengembangan AI-native sangat penting untuk meningkatkan produktivitas di lingkungan terdesentralisasi. Menurut Kasr, integrasi sistem cerdas ke dalam alur kerja pengembangan memungkinkan tim mengotomatiskan proses rutin dan fokus untuk membangun aplikasi terdesentralisasi yang skalabel dan efisien. Pengembangan ini sejalan dengan transisi yang lebih luas dari platform Web3 menuju arsitektur Web4, di mana otomatisasi yang digerakkan oleh AI, koordinasi cerdas, dan infrastruktur yang dapat dioperasikan mendukung sistem produktivitas terdesentralisasi yang lebih canggih. Tentang Atua AI adalah platform produktivitas AI terdesentralisasi yang menyediakan alat cerdas dan sistem otomatisasi untuk membantu pengembang, kreator, dan perusahaan membangun dan mengelola aplikasi di seluruh ekosistem blockchain.Kontak MediaKaJ Labsmedia@kajlabs.com88887012914730 University Way NE 104- #175https://kajlabs.com Sumber :Kajlabs Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Komite Olimpiade Melarang Atlet Transgender Mengikuti Acara untuk Wanita. Ini Penjelasan Kebijakan. Informasi

Komite Olimpiade Melarang Atlet Transgender Mengikuti Acara untuk Wanita. Ini Penjelasan Kebijakan.

(SeaPRwire) - Komite Olimpiade Internasional (IOC) pada hari Kamis mengumumkan bahwa atlet wanita transgender tidak akan diizinkan berpartisipasi dalam acara wanita.“Kelayakan untuk acara kategori wanita apa pun di Olimpiade atau acara IOC lainnya, termasuk olahraga individu dan tim, sekarang terbatas pada wanita biologis,” kata IOC. Kebijakan baru ini akan diterapkan mulai pada Olimpiade Musim Panas 2028 di Los Angeles. IOC mencatat bahwa “kebijakan ini tidak bersifat retroaktif dan tidak berlaku untuk program olahraga akar rumput atau rekreasi apa pun.”Presiden IOC Kirsty Coventry, mantan perenang Olimpiade, menyebut kebijakan ini “perlindungan kategori wanita” dan mengakui sifat “sangat sensitif” dari topik ini dalam video yang menyertai pengumuman IOC. White House merayakan keputusan ini, yang sejalan dengan Perintah Eksekutif yang ditandatangani Presiden Donald Trump setelah kembali ke White House tahun lalu, dan mengakui peran Trump dalam langkah ini—meskipun IOC tidak menyebut Presiden dalam pengumumannya.“Perintah Eksekutif Presiden Trump yang melindungi olahraga wanita membuat ini terjadi!” tulis Sekretaris Pers White House Karoline Leavitt di X.Namun, kelompok hak asasi manusia sebelumnya telah berbicara melawan penggunaan tes jenis kelamin untuk menentukan kelayakan atlet, dan organisasi advokasi telah mengutuk rencana IOC untuk mengembangkan persyaratan tes genetik dan melarang atlet transgender berkompetisi. Minggu lalu, sebelum pengumuman komite, puluhan kelompok mengecam langkah seperti ini sebagai “pengurangan yang mengejutkan terhadap kesetaraan gender” yang akan “membuat olahraga wanita mundur 30 tahun.”Berikut adalah hal-hal yang perlu diketahui tentang kebijakan baru komite Olimpiade.Bagaimana atlet akan disaring sesuai kebijakan baru? Sesuai kebijakan baru, “kelayakan untuk acara kategori wanita apa pun di Olimpiade atau acara IOC lainnya, termasuk olahraga individu dan tim, sekarang terbatas pada wanita biologis, yang ditentukan berdasarkan skrining gen SRY sekali seumur hidup,” tulis Olimpiade. Dalam dokumen 10 halaman yang menguraikan kebijakan ini, IOC menyatakan bahwa “cara paling akurat dan paling tidak mengganggu yang tersedia saat ini untuk menyaring jenis kelamin biologis adalah dengan menyaring Gen SRY, yang merupakan segmen DNA yang hampir selalu berada pada kromosom Y, memulai perkembangan jenis kelamin laki-laki di dalam rahim, dan menandakan keberadaan testis.”SRY, yang merupakan singkatan dari “sex determining region Y” (wilayah penentu jenis kelamin Y), digambarkan oleh IOC sebagai “skrining jenis kelamin biologis yang sangat akurat dan non-invasif,” yang dapat diperoleh menggunakan saliva, swab pipi, atau sampel darah. IOC mengatakan skrining ini akan menjadi “tes sekali seumur hidup” untuk atlet yang hasilnya negatif, kecuali dalam kasus di mana “ada alasan untuk percaya bahwa hasil negatif adalah kesalahan.”“Atlet yang hasil skrining gen SRY negatif secara permanen memenuhi kriteria kelayakan kebijakan ini untuk berkompetisi dalam kategori wanita,” kata komite. IOC menguraikan “pengecualian langka” terhadap kriteria kelayakan ini. Atlet dengan “diagnosis Sindrom Insensitivitas Androgen Lengkap (CAIS) atau perbedaan/kelainan langka lainnya dalam perkembangan jenis kelamin (DSDs) yang tidak mendapat manfaat dari efek anabolik dan/atau peningkat kinerja testosteron” akan tetap layak berkompetisi dalam kategori wanita meskipun hasil skrining SRY mereka positif. Semua yang lain dengan hasil skrining SRY positif akan dilarang berkompetisi dalam acara wanita.World Athletics, badan internasional yang mengatur kompetisi atletik termasuk lari dan lapangan, sebelumnya mengumumkan bahwa akan membutuhkan skrining gen SRY untuk menentukan kelayakan berpartisipasi dalam acara wanita. Organisasi olahraga lainnya juga telah mengadopsi bentuk tes gender.Mengapa IOC menerapkan larangan ini?Kebijakan baru IOC didasarkan pada temuan dari kelompok kerja yang dibentuk untuk menyelidiki “perlindungan kategori wanita” setelah rapat komite tahun lalu.“Ada dukungan yang luar biasa dari semua Anggota yang hadir di sini, dan mereka yang dapat berbagi dengan kami sebelum mereka pergi, bahwa kami harus melindungi kategori wanita,” kata Coventry pada saat itu. Kelompok kerja ini terdiri dari “spesialis dalam ilmu olahraga, endokrinologi, obat transgender, obat olahraga, kesehatan wanita, etika dan hukum,” menurut IOC, dan meninjau “bukti ilmiah terbaru, termasuk perkembangan sejak 2021,” serta melakukan wawancara dengan “atlet yang terpengaruh dari seluruh dunia.”Komite mengatakan pada hari Kamis bahwa berdasarkan pekerjaannya, kelompok tersebut telah “mencapai konsensus yang jelas” bahwa “jenis kelamin laki-laki memberikan keunggulan kinerja dalam semua olahraga dan acara yang bergantung pada kekuatan, daya, dan ketahanan.”“Bukti ilmiah sangat jelas. Kromosom laki-laki memberikan keunggulan kinerja dalam olahraga yang bergantung pada kekuatan, daya, atau ketahanan,” kata Coventry dalam video yang dibagikan bersama pengumuman pada hari Kamis. “Di Olimpiade, bahkan margin terkecil bisa menjadi perbedaan antara kemenangan dan kekalahan, jadi sangat jelas bahwa tidak adil bagi laki-laki biologis untuk berkompetisi dalam kategori wanita. Selain itu, dalam beberapa olahraga, itu tidak aman.”Tantangan dari advokatMinggu lalu, setelah laporan tentang rekomendasi kelompok kerja, 90 organisasi, termasuk International Commission of Jurists dan Sport & Rights Alliance, mengeluarkan pernyataan bersama yang mendesak IOC untuk tidak membutuhkan tes genetik bagi atlet atau melarang atlet transgender dari acara wanita.“Kebijakan tes jenis kelamin dan larangan total akan menjadi erosi bencana terhadap hak dan keamanan wanita,” kata Andrea Florence, Direktur Eksekutif Sport & Rights Alliance, dalam sebuah pernyataan. “Pengawasan gender dan eksklusi membahayakan semua wanita dan gadis, dan merusak martabat dan keadilan yang IOC klaim untuk menjunjung tinggi.”Organisasi tersebut mencatat bahwa badan-badan termasuk United Nations High Commissioner for Human Rights dan World Medical Association telah mengkritik penggunaan tes jenis kelamin dalam olahraga, dan mengatakan bahwa kebijakan ini juga akan bertentangan dengan Kerangka Kerja 2021 IOC sendiri tentang Keadilan, Inklusi, dan Non-Diskriminasi. Kelompok tersebut juga berpendapat dalam pernyataan bersama bahwa tes genetik wajib akan melanjutkan sejarah peraturan kelayakan olahraga yang secara tidak proporsional mempengaruhi wanita berwarna dari “Global South” dalam beberapa tahun terakhir.“IOC tidak boleh membelakangi wanita dan gadis berwarna,” kata medali Olimpiade Francine Niyonsaba dalam sebuah pernyataan. “Saya memberikan banyak waktu dan usaha untuk membangun Kerangka Kerja 2021 dan telah berulang kali berbagi pandangan saya. Saya harap IOC tidak akan mengabaikan kami.” Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Pencipta Something Very Bad Is Going to Happen, Haley Z. Boston, Menjelaskan Finale Serial Horor yang Berdarah Informasi

Pencipta Something Very Bad Is Going to Happen, Haley Z. Boston, Menjelaskan Finale Serial Horor yang Berdarah

(SeaPRwire) - Perhatian: Post ini mengandung spoiler untuk Something Very Bad Is Going to Happen.Awalnya, sepertinya satu jenis hal buruk akan terjadi. Lalu, hal buruk lainnya. Pada final Something Very Bad Is Going to Happen, hal buruk yang akan terjadi sudah sangat jelas. Tetapi itu tidak berarti protagonis kita yang ditakdirkan untuk gagal mampu menghentikannya.Diciptakan oleh showrunner Haley Z. Boston (yang sebelumnya menulis untuk Guillermo del Toro’s Cabinet of Curiosities dan Brand New Cherry Flavor) dan diproduksi eksekutif oleh Duffer Brothers (Stranger Things), seri horor Netflix baru ini, dengan delapan episode yang sekarang sudah dapat ditonton, menceritakan sepanjang minggu menjelang pernikahan yang malang dari pasangan calon suami istri Rachel Harkin (Camila Morrone) dan Nicky Cunningham (Adam DiMarco). Setelah perjalanan yang penuh kejadian mengerikan ke kompleks kabin terpencil keluarga Cunningham, Rachel awalnya percaya bahwa keluarga tunangannya—yang dia pertemukan untuk pertama kalinya—berencana untuk mengorbankan dirinya dalam ritual setan. Namun setelah perilaku aneh keluarga Cunningham sebagian besar dijelaskan oleh pengungkapan bahwa ibu Nicky, Victoria (Jennifer Jason Leigh), menderita tumor otak terminal yang mereka sembunyikan dari Nicky, Rachel terpaksa menghadapi bahaya supranatural yang sebenarnya mengintai dirinya."Paruh pertama seri, Rachel percaya ancamannya berasal dari luar. Lalu di tengah-tengah, dia menyadari ancamannya berasal dari dalam dirinya sendiri," kata Boston tentang penipuan awal ini. "Dia berpikir keluarga ini ingin menyakiti dia, ada kejahatan di hutan. Lalu dia menyadari bahwa ancamannya sebenarnya dirinya sendiri. Keraguan dirinya yang menyebabkan semua kecemasan ini. Ada sesuatu yang menarik tentang ingin menyalahkan orang lain tetapi akhirnya menyadari bahwa kamu harus melihat lebih dalam ke dalam dirimu sendiri untuk menghadapi ketakutanmu."Sebuah kutukan yang tak terbalik(Kiri-Kanan): Adam DiMarco sebagai Nicky dan Camila Morrone sebagai Rachel dalam Episode 5 Something Very Bad Is Going To Happen. —NetflixTernyata, keluarga Harkin telah terkutuk oleh kutukan yang menyebabkan anggota garis keturunan mana pun yang menikah dengan seseorang yang bukan soulmate sejatinya akan berdarah dalam jumlah besar dan mati begitu matahari terbenam pada hari pernikahan mereka. Rachel akhirnya mengetahui informasi ini dari lelaki tua seram (diperankan oleh Zlatko Burić) yang pertama kali dia temui menatapnya di kamar mandi bar selama perjalanan ke kabin. Lelaki itu, yang kita sebut sebagai Saksi dari sekarang, mengungkapkan bahwa kutukan itu diturunkan ke keluarga Rachel sebagai akibat dari keputusannya lama lalu untuk meninggalkan calon istrinya di altar. Dia memberi tahu Rachel bahwa kutukan itu berasal dari perjanjian yang dibuat buyut buyut buyutnya dengan Maut sendiri untuk membangkitkan kekasihnya yang sudah meninggal. Maut setuju, asalkan dia percaya bahwa kekasihnya yang sudah meninggal benar-benar soulmate-nya. Kemudian, untuk menambah, Maut juga memberkati semua anaknya, cucu-cucunya, dan seterusnya dengan beban yang sama. Setelah Saksi merasa ragu pada kekasihnya Marianne, dia akhirnya menikah dengan seorang pria bernama Thomas Harkin, buyut buyut buyut buyut buyut Rachel. Dengan demikian, kutukan itu diturunkan ke keluarga Harkin dan Saksi dihukum dengan keabadian karena mengkhianati perjanjian Maut. Sejak hari yang tak terlupakan itu, dia terpaksa menyaksikan semua pernikahan dalam garis keturunan Marianne. Seperti yang diberitahu Saksi kepada Rachel, halnya sederhana. Dia harus menikah sebelum matahari terbenam pada hari pernikahannya. Jika Nicky adalah soulmate-nya, dia akan hidup. Jika tidak, dia akan mati. Mengingat Rachel baru saja mengetahui bahwa inilah cara ibunya yang hamil dalam kondisi berat meninggal pada hari dia menikah dengan ayahnya—menyebabkan ayahnya melakukan operasi Caesar paksa pada tubuh ibunya yang tak bernyawa untuk menyelamatkan bayi Rachel—dia sudah tidak merasa baik-baik saja dengan situasi ini. "Saya percaya ada orang yang tepat dan orang yang salah. Saya tidak percaya pada sisi takdir," kata Boston tentang pendapatnya tentang soulmate. "Tetapi ketika saya mencoba menjawab pertanyaan tentang apa yang membuat seseorang soulmate, saya tidak ingin terlihat memiliki jawaban yang suci. Saya pikir orang yang tepat akan melihatmu seperti siapa kamu sebenarnya."Final berdarahPernikahan Rachel dan Nicky dimulai dalam Episode 8 Something Very Bad Is Going to Happen. —NetflixKeyakinan Rachel bahwa Nicky adalah soulmate-nya didorong oleh cerita awal mereka sebagai pasangan, yang berkisar pada keduanya tidak naik pesawat setelah tidak bisa melepaskan perasaan bahwa sesuatu yang buruk akan terjadi dan memilih untuk melakukan perjalanan empat hari ke tujuan akhir mereka bersama. Jadi ketika di malam persiapan pernikahan terungkap bahwa keadaan pertemuan romantis mereka di bandara semuanya adalah kebohongan, Rachel mulai memiliki keraguan yang serius. Pada hari pernikahan mereka tiba, Rachel siap menjalani ritual yang menyakitkan dan tak terbalik untuk memastikan dia benar-benar soulmate Nicky—bahkan jika itu mengubahnya menjadi orang yang berbeda sama sekali. Tetapi pada akhirnya, dia memutuskan untuk mempercayai hubungannya dengan Nicky dan melanjutkan upacara sebagai dirinya yang sebenarnya.Namun, Nicky selama ini juga merenungkan hubungan mereka dan akhirnya menolak menikahi Rachel di altar. Dia mengklaim ini karena dia merasa itu yang sebenarnya diinginkan Rachel, tetapi akhirnya dia mengakui dia juga tidak benar-benar percaya pada kutukan. Sayangnya, perjanjian Maut sangat nyata. Dan ketika matahari terbenam tanpa pasangan yang menikah, beban itu diturunkan ke garis keturunan Nicky, menyebabkan semua kerabat menikah non-soulmate yang hadir mulai berdarah dalam jumlah besar. Nicky kemudian mencoba memperbaiki kerusakan dengan memasukkan cincin ke jari Rachel dan berkata "saya setuju," menyelesaikan upacara tanpa izinnya untuk memaksa dia menikah. Hal ini, pada gilirannya, menyebabkan Rachel berdarah dan mati."Jika Nicky mengatakan ya di altar, jika dia hanya tenang dan tidak berkembang sama sekali, semuanya akan baik-baik saja," kata Boston. "Itulah tragedi besar dari final. Pada akhirnya, seri ini mengatakan bahwa dosa terbesar adalah tidak percaya bahwa orangmu adalah orang yang tepat untukmu."Keesokan paginya, Rachel bangun kembali, dibangkitkan kembali sebagai Saksi abadi baru yang sekarang harus menghadiri setiap pernikahan yang melibatkan anggota garis keturunan Cunningham. Adegan terakhir Something Very Bad menunjukkan Rachel mengemudi pergi dari kabin sendirian sebelum tersenyum lembut. "Seluruh cerita adalah cerita putus cinta. Jadi kematian Rachel adalah kematian hubungan. Itu kematian dirinya yang lama. Dan untuk terus hidup, dia harus lahir kembali," kata Boston. "Ketika kamu keluar dari hubungan, kamu meninggalkan semua itu dan bebas, meskipun tidak tanpa luka." Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Harga Saham Chewy (CHWY) Naik 13% Setelah Proyeksi Lebih Tinggi Dari Ramalan Wall Street – Waktunya Beli?

TLDR Saham Chewy naik ~13% setelah perusahaan mengeluarkan panduan pendapatan 2026 sebesar $13,6 miliar–$13,75 miliar, di atas perkiraan analis Pendapatan Q4 mencapai $3,26 miliar, naik 8,1% setelah disesuaikan dengan minggu tambahan di kuartal tahun lalu Pelanggan aktif tumbuh 4% menjadi 21,3 juta; penjualan bersih per pelanggan aktif naik 2,2% menjadi $591 Chewy mengharapkan penghematan biaya yang didorong AI sebesar $50 juta+ per tahun pada 2027, dengan manfaat “puluhan juta rendah” sudah diharapkan pada 2026 Chewy Vet Care sekarang memiliki 18 lokasi dan digambarkan sebagai segmen yang tumbuh paling cepat per pelanggan aktif (SeaPRwire) - Chewy mengumumkan hasil kuartal keempat pada hari Rabu yang sebagian besar memenuhi ekspektasi Wall Street, tetapi pandangan 2026lah yang membuat investor bergerak. Chewy, Inc., CHWY Pengecer suku cadang hewan peliharaan ini memberikan panduan pendapatan tahunan sebesar $13,6 miliar hingga $13,75 miliar. Ini melebihi konsensus analis sebesar $13,58 miliar dan membuat saham naik sekitar 13% pada hari itu, penutupan di sekitar $26,50. Pendapatan Q4 mencapai $3,26 miliar, naik 0,5% berdasarkan laporan dan 8,1% ketika disesuaikan dengan minggu tambahan di periode sebanding tahun lalu. Ini sesuai dengan perkiraan. Margin bruto meningkat 90 basis poin menjadi 29,4%, dan EBITDA disesuaikan naik dari $124,5 juta menjadi $162,3 juta. EPS disesuaikan mencapai $0,27, hanya satu sen di bawah konsensus $0,28. Pendapatan bersih GAAP sebesar $39,2 juta, atau $0,09 per saham, naik dari $22,8 juta tahun lalu. Pelanggan aktif tumbuh 4% tahun ke tahun menjadi 21,3 juta. Penjualan bersih per pelanggan aktif naik 2,2% menjadi $591. CEO Sumit Singh mencatat bahwa pemilik hewan peliharaan semakin memperlakukan hewan peliharaan seperti anggota keluarga dan beralih ke produk premium — tren yang dia harapkan akan berlanjut. CFO Chris Deppe mengatakan panduan 2026 tidak memasukkan inflasi harga apapun. Pertumbuhan diharapkan berasal dari penambahan pelanggan baru dan pengeluaran yang lebih tinggi per pelanggan yang sudah ada. Penghematan AI Mulai Terlihat Chewy telah membangun infrastruktur AI selama beberapa kuartal dan sekarang mulai menerapkannya di seluruh operasi, termasuk lapisan layanan, rantai pasok, dan jaringan pemenuhan pesanan. Singh mengatakan efisiensi yang didorong AI seharusnya memberikan manfaat “puluhan juta rendah” pada 2026, meningkat menjadi sekitar $50 juta atau lebih dalam penghematan tahunan pada 2027. Perusahaan juga meningkatkan operasi di pusat pemenuhan pesanan generasi berikutnya di Houston sebagai bagian dari upaya pengurangan biaya yang lebih luas. Untuk Q1 2026, Chewy memberikan panduan pendapatan sebesar $3,33 miliar hingga $3,36 miliar dan EPS disesuaikan sebesar $0,40–$0,45, yang secara luas sesuai dengan apa yang diharapkan analis. Perluasan Layanan Vet Care Berlanjut Chewy Vet Care menambahkan 10 lokasi baru pada tahun fiskal 2025, menjadikan total 18 praktik. CVC saat ini beroperasi di lima negara bagian, dengan rencana perluasan nasional. Singh mengatakan kinerja CVC melebihi ekspektasi dalam kepuasan pelanggan dan berfungsi sebagai alat akuisisi pelanggan yang memperkuat ikatan dengan pembeli berharga tinggi. Perusahaan menyebutnya sebagai segmen yang tumbuh paling cepat berdasarkan penjualan bersih per pelanggan aktif. Chewy juga menyelesaikan akuisisi SmartEquine, sebuah platform kesehatan kuda. Kesepakatan itu diharapkan menambah sekitar $80 juta dalam penjualan bersih pada 2026 — di bawah 1% dari total pendapatan, tetapi menandakan dorongan melampaui hewan peliharaan rumah tangga tradisional. Meskipun ada rally pada hari Rabu, saham Chewy telah kehilangan hampir 20% nilai nya selama 12 bulan terakhir dan tetap jauh di bawah tinggi 52 minggu nya sebesar $48,62.Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Saham Wave Life Sciences (WVE) Menurun 30% Meskipun Menyebut Data Uji Coba Obesitas “Positif”

TLDR Saham Wave Life Sciences turun 30% pada hari Kamis setelah merilis data interim Fase 1 dari uji coba obesitas INLIGHT-nya Dosis tunggal 240mg WVE-007 menghasilkan penurunan lemak visceral yang disesuaikan dengan placebo sebesar 14% selama enam bulan Peserta uji coba memiliki rata-rata BMI (32) yang lebih rendah daripada yang biasanya terlihat dalam studi obesitas, membatasi perbandingan langsung dengan pesaing Jefferies mempertahankan peringkat Buy dan target harga $28 pada WVE menjelang rilis data Wave berencana memulai Fase 2a INLIGHT pada Q2 2026, menargetkan pasien dengan BMI tinggi dengan komorbiditas (SeaPRwire) - Wave Life Sciences merilis data interim Fase 1 dari uji coba INLIGHT pada hari Kamis, dan pasar tidak terkesan. Saham turun 30% pada hari itu meskipun hasil yang disajikan perusahaan sebagai positif. Wave Life Sciences Ltd., WVE Data tersebut mencakup WVE-007, sebuah pengobatan untuk obesitas. Dosis tunggal 240mg menghasilkan penurunan lemak visceral yang disesuaikan dengan placebo sebesar 14% selama enam bulan pada peserta dengan rata-rata BMI 32 kg/m². Perusahaan juga melaporkan peningkatan 16,5% pada rasio lemak visceral terhadap otot dari garis dasar. Massa tanpa lemak meningkat 2,4%, lingkar pinggang turun 3,3%, dan berat badan turun 0,9% berdasarkan penyesuaian placebo. WVE-007 ditoleransi dengan baik hingga 600mg. Tidak ada penghentian pengobatan atau kejadian advers berat. Penurunan Serum Activin E bertahan setidaknya tujuh bulan, mendukung potensi dosis sekali atau dua kali setahun. Masalahnya? Rata-rata BMI dalam kohort ini adalah 32 — jauh di bawah 37 yang biasanya terlihat dalam uji coba obesitas Fase 2 dan 3. Hal ini membuat perbandingan dengan obat lain yang sedang dikembangkan menjadi lebih sulit. Wave membandingkan hasil lemak visceral WVE-007 dengan semaglutide mingguan dari uji coba Fase 2 terpisah. Studi semaglutide tersebut merekrut pasien dengan BMI yang lebih tinggi, sehingga perbandingan tersebut menimbulkan pertanyaan. Investor kemungkinan besar mempertimbangkan keterbatasan tersebut di tengah latar belakang pasar obat obesitas yang sangat kompetitif saat ini dipimpin oleh Novo Nordisk dan Eli Lilly. Phase 2a Incoming Wave berencana memulai bagian Fase 2a INLIGHT pada Q2 2026. Studi tersebut akan merekrut pasien dengan BMI 35–50 dengan komorbiditas — populasi uji coba obesitas yang lebih khas. Perusahaan mengharapkan kohort dengan BMI lebih tinggi untuk menunjukkan hasil komposisi tubuh dan penurunan berat badan yang lebih kuat. Data dari studi tersebut akan menginformasikan strategi pengembangan Wave di bidang obesitas, MASH, diabetes tipe 2, dan penyakit kardiovaskular. Hanya satu hari sebelum rilis data, Jefferies telah mengulangi peringkat Buy dan target harga $28 pada WVE, dengan menyebutkan pendekatan pengeditan RNA dan program INHBE sebagai pendorong utama. Analis Roger Song menandai potensi keunggulan platform Wave: tidak ada pengeditan di luar target, profil keamanan yang lebih bersih, dan efek yang tahan lama dengan dosis ulang yang nyaman. Other Pipeline Updates Secara terpisah, Wave mendapatkan kembali hak penuh atas WVE-006 dari GSK. Perusahaan akan mempresentasikan poster di ADA dan berharap untuk merilis pembaruan dosis meningkat ganda 400mg dan dosis tunggal meningkat 600mg pada Mei. Mizuho menaikkan target harga pada WVE menjadi $27 dari $22 awal tahun ini, dengan mempertahankan peringkat Outperform setelah Wave mengambil alih kepemilikan penuh WVE-006. Wave juga melaporkan laba Q4 dan tahun penuh 2025 baru-baru ini, mencatat tekanan keuangan dari berakhirnya kolaborasi besar. Pendapatan melampaui perkiraan, tetapi EPS meleset dari ekspektasi. Perusahaan memegang kas lebih banyak daripada utang di neracanya, menurut data InvestingPro. Data dari uji coba RestorAATion-2 WVE-006 akan dipresentasikan di American Thoracic Society International Conference pada tahun 2026, mencakup kohort multidosis 400mg dan dosis tunggal 600mg.Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Saham Intel dan AMD Melonjak karena Kenaikan Harga CPU Mendorong Rally Chip

TLDR Saham Intel dan AMD masing-masing naik sekitar 7% pada Rabu setelah laporan tentang rencana peningkatan harga CPU sebesar 10–15% Nikkei Asia melaporkan kedua perusahaan tersebut memberitahu pelanggan bahwa harga akan naik mulai Maret dan April Intel menyebutkan “permintaan yang berkelanjutan, peningkatan biaya komponen dan bahan baku” sebagai alasan peningkatan harga Hal ini mengikuti beberapa peningkatan harga sebelumnya tahun ini, dengan waktu tunggu pengiriman juga meningkat Indeks semikonduktor yang lebih luas naik 1%, dengan Nvidia, Marvell, dan Qualcomm juga mencatat kenaikan (SeaPRwire) - Saham Intel dan AMD melonjak tajam pada Rabu setelah laporan mengatakan kedua pembuat chip tersebut sedang menaikkan harga unit pemroses pusat mereka. Langkah ini mendorong kedua saham tersebut ke puncak daftar performer harian S&P 500. Advanced Micro Devices, Inc., AMD Nikkei Asia melaporkan bahwa Intel dan AMD memberitahu pelanggan mereka berencana menaikkan harga di seluruh lini produk CPU mereka. Peningkatan tersebut dijadwalkan dimulai Maret dan April, dengan peningkatan rata-rata 10% hingga 15%. Beberapa produk diperkirakan akan mengalami penyesuaian yang lebih besar. Intel mengkonfirmasi perubahan tersebut dalam pernyataan kepada Investopedia. Seorang juru bicara mengatakan penyesuaian harga mencerminkan “permintaan yang berkelanjutan, peningkatan biaya komponen dan bahan baku, serta dinamika pasar yang berkembang.” AMD tidak menanggapi permintaan komentar. Saham Intel naik sekitar 7% pada perdagangan Rabu. Saham tersebut sekarang telah naik hampir 20% pada tahun 2026 hingga saat ini, sebagian didorong oleh optimism tentang dukungan pemerintah untuk manufaktur chip domestik dan rumor tentang kesepakatan klien baru. Saham AMD juga naik sekitar 7% pada hari itu. Namun, saham tersebut masih turun sekitar 4% selama tahun ini memasuki sesi Rabu. Investor memiliki kekhawatiran tentang kemampuan AMD untuk bersaing dengan Nvidia di pasar chip AI. Mengapa Harga Chip Naik Ini bukan pertama kalinya Intel dan AMD menaikkan harga tahun ini. Kedua perusahaan tersebut telah beberapa kali menaikkan harga pada tahun 2026, karena kendala pasokan menjadi lebih ketat. Waktu tunggu pengiriman juga telah meningkat, menurut laporan Nikkei Asia. Permintaan akan chip tetap kuat di kedua pasar konsumen dan enterprise. Harga yang lebih tinggi, dikombinasikan dengan permintaan yang stabil, dapat meningkatkan pendapatan dan margin laba untuk kedua perusahaan. Indeks Semikonduktor PHLX naik 1% pada Rabu. Nvidia, Marvell Technology, dan Qualcomm juga mencatat kenaikan bersama dengan Intel dan AMD. Pasar Lebih Luas Juga Mendukung Rally Di luar berita khusus chip, pasar yang lebih luas bergerak ke atas pada Rabu. Futures S&P 500 naik sekitar 0.6% setelah laporan bahwa AS menyusun rencana untuk menghentikan pertempuran di Timur Tengah. Harga minyak turun 5% ke bawah $100 per barel. Hal itu meredakan beberapa kekhawatiran tentang inflasi yang didorong energi, yang telah menjadi beban bagi saham tech minggu-minggu terakhir. AMD juga memiliki beberapa dorongan khusus perusahaan. Perusahaan tersebut baru-baru ini mengumumkan kesepakatan dengan Meta untuk menerapkan 6 gigawatt unit pemroses grafis. Kesepakatan itu menambah sentimen positif seputar prospek bisnis AMD. Saham Intel memasuki Rabu dengan momentum tahun-hingga-sekarang yang kuat, sementara AMD sedang mencoba memulihkan posisi yang hilang. Berita peningkatan harga CPU memberinya dorongan kepada kedua saham pada hari yang sama. Waktu tunggu pengiriman untuk prosesor telah meningkat seiring dengan peningkatan harga, menurut laporan Nikkei Asia, yang mencerminkan kondisi pasokan yang lebih ketat di seluruh industri chip.Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Saham Merck (MRK) naik sedikit karena akuisisi Terns senilai $6,7B meningkatkan outlook pipelain kanker

TLDRs; Saham Merck naik setelah mengumumkan kesepakatan akuisisi Terns senilai $6.7 miliar Kedaluwarsa paten Keytruda mendorong strategi ekspansi onkologi yang agresif Terapi leukemia TERN-701 menjadi aset inti dalam pipeline Investor menimbang premi yang relatif kecil terhadap pertumbuhan jangka panjang pipeline kanker (SeaPRwire) - Saham Merck & Co. (NYSE: MRK) naik sedikit setelah perusahaan mengumumkan akuisisi penuh tunai senilai $6.7 miliar atas Terns Pharmaceuticals (NASDAQ: TERN). Kesepakatan ini, dengan harga $53 per saham, menandakan upaya baru dari raksasa farmasi ini untuk memperkuat pipeline onkologinya sambil mempersiapkan diri untuk kedaluwarsa paten obat kanker andalan Keytruda yang akan datang. Tanggapan pasar mencerminkan optimisme hati-hati, di mana investor melihat akuisisi ini sebagai langkah strategis untuk mengamankan aliran pendapatan masa depan di tengah persaingan yang semakin ketat di bidang onkologi. Tekanan dari Keytruda Mendorong Strategi Akuisisi ini terjadi pada saat kritis bagi Merck, karena Keytruda, obat imunoterapi terlarisnya, menghadapi kedaluwarsa paten yang diantisipasi mulai tahun 2028. Pada tahun 2025 saja, Keytruda menghasilkan pendapatan lebih dari $30 miliar, yang mencakup hampir setengah dari total penjualan Merck. Merck & Co., Inc., MRK Dengan ketergantungan yang besar pada satu aset, Merck telah mempercepat upaya untuk mendiversifikasi portofolio onkologinya. Kesepakatan dengan Terns merupakan langkah terukur ke arah itu, bertujuan untuk mengurangi ketergantungan jangka panjang pada Keytruda sambil memperkuat posisinya dalam kategori pengobatan kanker yang sedang berkembang. TERN-701 Menjadi Aset Inti Pada inti akuisisi ini terdapat TERN-701, terapi oral eksperimental yang menargetkan leukemia myeloid kronis, suatu jenis kanker darah dan sumsum tulang. Data klinis tahap awal menunjukkan hasil yang menjanjikan, dengan laporan menunjukkan tingkat respons sekitar 75% di antara pasien yang telah diobati sebelumnya. Para pemimpin riset Merck telah menggambarkan kinerja awal obat ini sebagai menggembirakan, menyarankan bahwa obat ini dapat menawarkan pendekatan yang berbeda dalam segmen pengobatan kanker darah yang kompetitif. Jika berhasil dalam uji klinis tahap lanjut, TERN-701 dapat menempatkan Merck dalam persaingan langsung dengan terapi yang sudah mapan dan mendominasi pasar. Tanggapan Pasar dan Perdebatan Nilai Meskipun besarnya kesepakatan, premi langsung yang ditawarkan kepada pemegang saham Terns tampak relatif kecil, dengan penawaran hanya menunjukkan kenaikan persentase satu digit dari level perdagangan terbaru. Namun, saham Terns melonjak dalam perdagangan pra-pasar saat investor bereaksi terhadap kepastian akuisisi tersebut. Analis mencatat bahwa meskipun nilai tersebut mungkin meninggalkan ruang untuk perdebatan, nilai strategis aset pipeline lebih mengatasi kekhawatiran harga jangka pendek. Namun, beberapa pengamat menyarankan bahwa premi yang terbatas dapat menarik minat dari penawar alternatif, meskipun belum ada penawaran saing yang muncul sejauh ini. Strategi Akuisisi Lebih Luas Diperluas Kesepakatan dengan Terns merupakan yang terbaru dalam serangkaian akuisisi oleh Merck yang bertujuan untuk memperkuat prospek pertumbuhan jangka panjang. Selama tahun lalu, perusahaan telah menyelesaikan beberapa transaksi di bidang bioteknologi dan farmasi khusus, semuanya dirancang untuk membangun kedalaman di luar Keytruda. Langkah-langkah ini merupakan bagian dari upaya restrukturisasi yang lebih luas dalam divisi kesehatan manusia Merck, yang baru-baru ini memisahkan operasinya menjadi unit yang berfokus pada onkologi dan non-onkologi. Perubahan ini menyoroti peran sentral pengobatan kanker dalam strategi perusahaan, bahkan saat perusahaan mengeksplorasi bidang terapi tambahan. Prospek Meskipun akuisisi ini masih memerlukan persetujuan regulator dan dukungan pemegang saham, sentimen pasar menunjukkan kepercayaan yang meningkat terhadap rencana jangka panjang onkologi Merck. Investor sekarang memperhatikan dengan seksama apakah TERN-701 dapat berhasil melalui uji klinis dan membenarkan perannya sebagai landasan masa depan portofolio kanker Merck.Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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Indonesian Online Gambling Deposits Spike After Eid Holiday for Second Consecutive Year iGame

Indonesian Online Gambling Deposits Spike After Eid Holiday for Second Consecutive Year

(AsiaGameHub) - Officials report that Indonesian online gambling deposits are surging following the Muslim holiday of Eid al-Fitr for the second consecutive year. The alert was issued by the country's anti-money laundering body, the Financial Transaction Reports and Analysis Center (PPATK), according to Indonesian news outlet Tempo. PPATK runs an automated system that monitors transactions to detect online gambling activity in bank accounts. The agency collaborates with major Indonesian banks to freeze accounts identified as having gambling-related deposits or withdrawals. According to PPATK officials, there was a "sharp" rise in suspicious transactions potentially linked to online gambling both during and right after the Eid al-Fitr holiday. This year, Eid was observed by the Islamic world from March 19 to March 20. Inside a mosque in Central Java, Indonesia. (Image: Ed Us) Online Gambling Deposits: On the Rise The agency declined to disclose the precise magnitude of the increase, stating that official data would be released in April. Nevertheless, it noted that the figures from late March were substantially higher than those recorded in January and February. Experts informed the media outlet that increased leisure time during the holiday contributed to higher gambling activity. PPATK head Ivan Yustiavandana affirmed that "online gambling deposits generally rise following the conclusion of the holiday." "The [sharpest] upward trend usually occurs after Eid, when money circulation increases nationwide," he said. Upward Trends Statistics from 2025, when Eid occurred on March 29-30, seem to support the PPATK's assertion. In January 2025, Indonesian players placed deposits totaling IDR 2.96 trillion ($175 million) on unlawful betting sites. Deposits grew marginally to IDR 3.05 trillion ($180 million) the next month. Transaction values fell to IDR 2.59 trillion in March. However, April witnessed a 96% surge in deposits to IDR 5.08 trillion ($300 million), which then declined to IDR 2.29 trillion ($153 million) in May 2025. Gambling in all its forms is prohibited in Indonesia. Despite the prohibition, online casino applications continue to be widely used, prompting authorities to launch an extensive enforcement campaign in recent years. The enforcement actions have also generated substantial revenue for the Indonesian Treasury. Prosecutors in West Jakarta recently transferred approximately $31.3 million to government accounts following the closure of an online casino and its connected money-laundering operation. Medical professionals caution that the growing popularity of online gambling is increasingly impacting public mental health. Psychiatric units in major Indonesian urban centers report being inundated with admissions of patients battling gambling dependency. Certain regions report hospitals operating at 90% occupancy. Physicians indicate this is contributing to rising gambling-associated crime. Additionally, courts across the country have expressed concerns that addiction to unlawful casino platforms is causing divorce rates to climb. This article is provided by a third-party. AsiaGameHub (https://asiagamehub.com/) makes no warranties regarding its content. AsiaGameHub delivers targeted distribution for iGaming, Casino, and eSports, connecting 3,000+ premium Asian media outlets and 80,000+ specialized influencers across ASEAN.
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Saham Super Micro (SMCI) Turun 33% Setelah Tuduhan Penyelundupan DOJ Picu Gugatan Pemegang Saham

TLDR Pemegang saham mengajukan gugatan class action terhadap Super Micro Computer (SMCI) di pengadilan federal San Francisco Gugatan tersebut mengklaim SMCI menyembunyikan bahwa sebagian besar penjualan servernya ditujukan ke perusahaan-perusahaan China, melanggar hukum ekspor AS Saham SMCI turun 33% pada 20 Maret setelah Departemen Kehakiman (DOJ) mengumumkan dakwaan penyelundupan pidana terhadap pendiri bersama Yih-Shyan Liaw dan dua orang lainnya Skema penyelundupan yang diduga melibatkan server bertenaga Nvidia senilai $2,5 miliar penjualan sepanjang 2024 dan 2025 Analis telah memotong target harga, dengan Wall Street memegang peringkat konsensus "Hold" dan target rata-rata $31,70 (SeaPRwire) - Super Micro Computer mengalami minggu yang sulit — dan itu tidak menjadi lebih mudah. Super Micro Computer, Inc., SMCI Pemegang saham mengajukan gugatan class action di pengadilan federal San Francisco pada hari Rabu, menuduh pembuat server AI tersebut melakukan penipuan sekuritas. Gugatan itu mengklaim SMCI secara sengaja menyembunyikan bahwa sebagian besar pendapatan servernya berasal dari penjualan ke perusahaan-perusahaan China, yang melanggar hukum kontrol ekspor AS. Keluhan tersebut mencatat nama CEO Charles Liang dan CFO David Weigand sebagai terdakwa bersama bersama perusahaan. Gugatan ini menargetkan investor yang membeli saham SMCI antara 30 April 2024 dan 19 Maret 2026. Gugatan ini menuntut ganti rugi yang tidak ditentukan jumlahnya. Semua ini menyusul aksi jual dramatis pada 20 Maret. Saham SMCI anjlok 33% dalam satu sesi perdagangan setelah Departemen Kehakiman (DOJ) mengumumkan dakwaan penyelundupan pidana terhadap pendiri bersama dan direktur Yih-Shyan Liaw, manajer penjualan Taiwan Ruei-Tsang Chang, dan kontraktor Ting-Wei Sun. Menurut jaksa DOJ, Liaw dan Chang menggunakan perusahaan Asia Tenggara yang tidak disebutkan namanya sebagai perantara untuk menjual server bertenaga Nvidia ke pembeli terbatas di China. Skema yang diduga tersebut menghasilkan penjualan server senilai $2,5 miliar selama 2024 dan 2025. Super Micro sendiri belum disebut sebagai terdakwa dalam kasus DOJ. Perusahaan mengatakan telah "bekerja sama sepenuhnya" dengan penyelidikan pemerintah. Namun, hal itu tidak menghentikan gugatan pemegang saham untuk diajukan. Keluhan tersebut menuduh SMCI melebih-lebihkan prospek bisnisnya dan dengan sengaja menyembunyikan kelemahan material dalam kontrol kepatuhan ekspornya. Analis Memotong Target Harga Dampak dari kasus ini telah mendorong beberapa analis Wall Street untuk merevisi pandangan mereka. Analis Rosenblatt Securities Kevin Cassidy memangkas target harganya menjadi $32 dari $50, sambil mempertahankan peringkat Buy. Dia mengatakan kontroversi ini menempatkan "awan gelap" di atas periode pengumuman produk yang seharusnya kuat. Dia masih melihat backlog pesanan SMCI sehat tetapi memperkirakan saham akan tetap di bawah tekanan hingga penyelidikan selesai. Ruplu Bhattacharya dari Bank of America kurang memaafkan. Dia memotong targetnya menjadi $24 dari $34 dan mempertahankan peringkat Sell. Dia menandai risiko termasuk pemasok yang membatasi akses komponen, pelanggan yang menjeda pesanan, dan potensi pesaing untuk mengambil alih kontrak yang terganggu. Posisi Wall Street Saat Ini Saat ini, Wall Street memiliki peringkat konsensus Hold pada SMCI. Itu didasarkan pada delapan panggilan Hold, tiga Buy, dan tiga Sell. Target harga rata-rata berada di $31,70, menyiratkan kenaikan sekitar 32% dari level saat ini. Saham SMCI turun sekitar 18% year-to-date menjelang hari-hari terakhir bulan Maret.Artikel ini disediakan oleh penyedia konten pihak ketiga. SeaPRwire (https://www.seaprwire.com/) tidak memberikan jaminan atau pernyataan sehubungan dengan hal tersebut. Sektor: Top Story, Daily News SeaPRwire menyediakan distribusi siaran pers real-time untuk perusahaan dan lembaga, menjangkau lebih dari 6.500 toko media, 86.000 editor dan jurnalis, dan 3,5 juta desktop profesional di 90 negara. SeaPRwire mendukung distribusi siaran pers dalam bahasa Inggris, Korea, Jepang, Arab, Cina Sederhana, Cina Tradisional, Vietnam, Thailand, Indonesia, Melayu, Jerman, Rusia, Prancis, Spanyol, Portugis dan bahasa lainnya.
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